| Negative regulation of NMDA receptor-mediated neuronal transmission | 11 | 4.98e-03 | 0.11400 | 0.71300 | 5.65e-01 | 0.435000 | 1.18e-03 | 1.26e-02 | 
| Purine catabolism | 10 | 2.31e-02 | 0.22800 | 0.65400 | -4.48e-01 | -0.476000 | 1.41e-02 | 9.17e-03 | 
| Long-term potentiation | 10 | 5.54e-03 | 0.11500 | 0.64500 | 5.71e-01 | 0.301000 | 1.78e-03 | 9.89e-02 | 
| p75NTR signals via NF-kB | 11 | 1.99e-02 | 0.22200 | 0.63600 | -4.61e-01 | -0.439000 | 8.19e-03 | 1.18e-02 | 
| Ras activation upon Ca2+ influx through NMDA receptor | 10 | 5.56e-02 | 0.37000 | 0.56800 | 4.26e-01 | 0.376000 | 1.96e-02 | 3.96e-02 | 
| Meiotic recombination | 19 | 3.57e-03 | 0.10400 | 0.56100 | -3.45e-01 | -0.443000 | 9.30e-03 | 8.38e-04 | 
| Resolution of D-loop Structures through Holliday Junction Intermediates | 24 | 6.38e-04 | 0.05860 | 0.54700 | -4.52e-01 | -0.308000 | 1.26e-04 | 9.01e-03 | 
| Defective HDR through Homologous Recombination (HRR) due to BRCA1 loss-of-function | 19 | 2.24e-03 | 0.07500 | 0.53800 | -4.59e-01 | -0.282000 | 5.35e-04 | 3.36e-02 | 
| Defective HDR through Homologous Recombination (HRR) due to PALB2 loss of function | 19 | 2.24e-03 | 0.07500 | 0.53800 | -4.59e-01 | -0.282000 | 5.35e-04 | 3.36e-02 | 
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | 19 | 2.24e-03 | 0.07500 | 0.53800 | -4.59e-01 | -0.282000 | 5.35e-04 | 3.36e-02 | 
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | 19 | 2.24e-03 | 0.07500 | 0.53800 | -4.59e-01 | -0.282000 | 5.35e-04 | 3.36e-02 | 
| Impaired BRCA2 binding to PALB2 | 19 | 2.24e-03 | 0.07500 | 0.53800 | -4.59e-01 | -0.282000 | 5.35e-04 | 3.36e-02 | 
| Resolution of D-Loop Structures | 25 | 5.03e-04 | 0.05860 | 0.53800 | -4.49e-01 | -0.296000 | 1.01e-04 | 1.05e-02 | 
| Potassium Channels | 23 | 4.78e-03 | 0.11200 | 0.51400 | 3.51e-01 | 0.374000 | 3.55e-03 | 1.89e-03 | 
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 21 | 3.69e-03 | 0.10500 | 0.51300 | -4.22e-01 | -0.291000 | 8.18e-04 | 2.09e-02 | 
| RORA activates gene expression | 11 | 1.35e-02 | 0.19000 | 0.51100 | 4.72e-01 | 0.195000 | 6.73e-03 | 2.62e-01 | 
| Impaired BRCA2 binding to RAD51 | 30 | 1.73e-03 | 0.07500 | 0.48900 | -3.63e-01 | -0.327000 | 5.80e-04 | 1.96e-03 | 
| IKK complex recruitment mediated by RIP1 | 17 | 2.42e-02 | 0.23100 | 0.48200 | -2.96e-01 | -0.380000 | 3.50e-02 | 6.63e-03 | 
| Glycogen synthesis | 11 | 1.05e-01 | 0.45600 | 0.48000 | -3.58e-01 | -0.319000 | 3.96e-02 | 6.69e-02 | 
| A tetrasaccharide linker sequence is required for GAG synthesis | 10 | 9.92e-02 | 0.44600 | 0.47800 | 3.93e-01 | 0.273000 | 3.16e-02 | 1.35e-01 | 
| SARS-CoV-2 modulates autophagy | 10 | 1.34e-01 | 0.49100 | 0.46500 | -2.90e-01 | -0.363000 | 1.12e-01 | 4.67e-02 | 
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 25 | 7.14e-03 | 0.13500 | 0.45800 | -3.62e-01 | -0.281000 | 1.75e-03 | 1.51e-02 | 
| Signaling by Leptin | 10 | 2.84e-02 | 0.24600 | 0.45500 | 1.45e-01 | 0.431000 | 4.27e-01 | 1.82e-02 | 
| Mitochondrial tRNA aminoacylation | 17 | 3.69e-02 | 0.29500 | 0.44600 | -2.63e-01 | -0.360000 | 6.08e-02 | 1.02e-02 | 
| DCC mediated attractive signaling | 11 | 6.42e-03 | 0.12700 | 0.44300 | 4.37e-01 | 0.069800 | 1.20e-02 | 6.89e-01 | 
| Pexophagy | 11 | 1.37e-01 | 0.49100 | 0.44200 | -3.44e-01 | -0.277000 | 4.81e-02 | 1.12e-01 | 
| Signaling by BMP | 14 | 4.29e-03 | 0.11200 | 0.44200 | 1.08e-01 | 0.428000 | 4.85e-01 | 5.53e-03 | 
| Signaling by WNT in cancer | 22 | 2.32e-02 | 0.22800 | 0.44100 | 3.08e-01 | 0.316000 | 1.23e-02 | 1.04e-02 | 
| Caspase activation via Death Receptors in the presence of ligand | 10 | 1.78e-01 | 0.51900 | 0.43900 | -2.90e-01 | -0.330000 | 1.12e-01 | 7.11e-02 | 
| Translesion Synthesis by POLH | 16 | 6.45e-02 | 0.37900 | 0.43900 | -2.92e-01 | -0.327000 | 4.33e-02 | 2.35e-02 | 
| Signaling by Hippo | 10 | 8.11e-02 | 0.41600 | 0.43800 | 3.93e-01 | 0.195000 | 3.16e-02 | 2.85e-01 | 
| Activation of kainate receptors upon glutamate binding | 15 | 7.67e-02 | 0.40600 | 0.43700 | 2.87e-01 | 0.329000 | 5.47e-02 | 2.72e-02 | 
| TICAM1, RIP1-mediated IKK complex recruitment | 17 | 5.94e-02 | 0.37200 | 0.43300 | -2.92e-01 | -0.320000 | 3.72e-02 | 2.25e-02 | 
| Presynaptic phase of homologous DNA pairing and strand exchange | 32 | 5.18e-03 | 0.11500 | 0.43200 | -3.14e-01 | -0.297000 | 2.10e-03 | 3.67e-03 | 
| Negative regulation of FLT3 | 10 | 1.93e-01 | 0.53900 | 0.43200 | -2.96e-01 | -0.315000 | 1.06e-01 | 8.48e-02 | 
| Mucopolysaccharidoses | 10 | 1.54e-01 | 0.51200 | 0.42900 | 2.44e-01 | 0.353000 | 1.81e-01 | 5.32e-02 | 
| Assembly and cell surface presentation of NMDA receptors | 12 | 1.43e-01 | 0.49100 | 0.42900 | 2.98e-01 | 0.309000 | 7.42e-02 | 6.37e-02 | 
| Interleukin-10 signaling | 12 | 1.40e-01 | 0.49100 | 0.42500 | 2.76e-01 | 0.324000 | 9.85e-02 | 5.21e-02 | 
| tRNA Aminoacylation | 22 | 1.19e-02 | 0.17500 | 0.42400 | -2.19e-01 | -0.363000 | 7.53e-02 | 3.21e-03 | 
| Mitochondrial calcium ion transport | 14 | 1.01e-01 | 0.44900 | 0.42300 | 2.69e-01 | 0.326000 | 8.11e-02 | 3.47e-02 | 
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 33 | 5.37e-03 | 0.11500 | 0.42100 | -3.16e-01 | -0.278000 | 1.69e-03 | 5.66e-03 | 
| Diseases of DNA Double-Strand Break Repair | 33 | 5.37e-03 | 0.11500 | 0.42100 | -3.16e-01 | -0.278000 | 1.69e-03 | 5.66e-03 | 
| RHO GTPases activate CIT | 14 | 1.07e-01 | 0.45900 | 0.42000 | -2.73e-01 | -0.319000 | 7.66e-02 | 3.87e-02 | 
| Defects in vitamin and cofactor metabolism | 16 | 6.73e-02 | 0.38200 | 0.41800 | -3.35e-01 | -0.250000 | 2.04e-02 | 8.33e-02 | 
| Chaperone Mediated Autophagy | 12 | 1.50e-01 | 0.50500 | 0.41500 | -2.63e-01 | -0.321000 | 1.15e-01 | 5.44e-02 | 
| Ion homeostasis | 25 | 4.66e-03 | 0.11200 | 0.41400 | 3.67e-01 | 0.193000 | 1.51e-03 | 9.52e-02 | 
| HDR through Homologous Recombination (HRR) | 55 | 2.39e-04 | 0.04660 | 0.41400 | -3.06e-01 | -0.280000 | 8.89e-05 | 3.38e-04 | 
| HDMs demethylate histones | 15 | 6.54e-02 | 0.37900 | 0.41400 | -2.26e-01 | -0.347000 | 1.29e-01 | 1.99e-02 | 
| Processing of Intronless Pre-mRNAs | 15 | 4.64e-02 | 0.33800 | 0.41400 | -2.02e-01 | -0.362000 | 1.77e-01 | 1.53e-02 | 
| Rap1 signalling | 11 | 1.76e-01 | 0.51600 | 0.41200 | -3.22e-01 | -0.257000 | 6.44e-02 | 1.40e-01 | 
| Ephrin signaling | 11 | 1.12e-01 | 0.46300 | 0.41100 | 3.57e-01 | 0.202000 | 4.02e-02 | 2.46e-01 | 
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 15 | 9.44e-02 | 0.43600 | 0.41000 | -2.53e-01 | -0.322000 | 9.03e-02 | 3.08e-02 | 
| NRIF signals cell death from the nucleus | 13 | 6.22e-02 | 0.37900 | 0.40900 | -3.64e-01 | -0.187000 | 2.31e-02 | 2.44e-01 | 
| Removal of the Flap Intermediate from the C-strand | 15 | 1.17e-01 | 0.46600 | 0.40100 | -3.00e-01 | -0.266000 | 4.45e-02 | 7.46e-02 | 
| RIPK1-mediated regulated necrosis | 24 | 1.74e-02 | 0.21200 | 0.39800 | -2.16e-01 | -0.334000 | 6.68e-02 | 4.58e-03 | 
| Regulation of necroptotic cell death | 24 | 1.74e-02 | 0.21200 | 0.39800 | -2.16e-01 | -0.334000 | 6.68e-02 | 4.58e-03 | 
| Degradation of cysteine and homocysteine | 10 | 1.53e-01 | 0.51100 | 0.39700 | -3.46e-01 | -0.194000 | 5.79e-02 | 2.89e-01 | 
| VxPx cargo-targeting to cilium | 16 | 1.00e-01 | 0.44900 | 0.39700 | 3.05e-01 | 0.254000 | 3.48e-02 | 7.87e-02 | 
| Activation of G protein gated Potassium channels | 10 | 1.95e-01 | 0.53900 | 0.39700 | 2.20e-01 | 0.330000 | 2.28e-01 | 7.09e-02 | 
| G protein gated Potassium channels | 10 | 1.95e-01 | 0.53900 | 0.39700 | 2.20e-01 | 0.330000 | 2.28e-01 | 7.09e-02 | 
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 10 | 1.95e-01 | 0.53900 | 0.39700 | 2.20e-01 | 0.330000 | 2.28e-01 | 7.09e-02 | 
| mRNA 3’-end processing | 30 | 1.43e-02 | 0.19600 | 0.39500 | -2.54e-01 | -0.302000 | 1.59e-02 | 4.18e-03 | 
| Cytosolic sulfonation of small molecules | 10 | 2.25e-01 | 0.58200 | 0.39500 | 2.38e-01 | 0.315000 | 1.92e-01 | 8.47e-02 | 
| Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon | 13 | 1.33e-01 | 0.49100 | 0.39400 | -3.22e-01 | -0.227000 | 4.47e-02 | 1.57e-01 | 
| Golgi Cisternae Pericentriolar Stack Reorganization | 14 | 1.10e-01 | 0.46300 | 0.39300 | -2.23e-01 | -0.324000 | 1.49e-01 | 3.58e-02 | 
| Cardiac conduction | 40 | 1.73e-03 | 0.07500 | 0.39300 | 3.26e-01 | 0.220000 | 3.67e-04 | 1.61e-02 | 
| G beta:gamma signalling through PLC beta | 11 | 1.75e-01 | 0.51400 | 0.39000 | 3.25e-01 | 0.216000 | 6.24e-02 | 2.16e-01 | 
| Presynaptic function of Kainate receptors | 11 | 1.75e-01 | 0.51400 | 0.39000 | 3.25e-01 | 0.216000 | 6.24e-02 | 2.16e-01 | 
| Cell-cell junction organization | 12 | 1.69e-01 | 0.51200 | 0.38800 | 2.27e-01 | 0.315000 | 1.73e-01 | 5.93e-02 | 
| VLDLR internalisation and degradation | 11 | 2.22e-01 | 0.58000 | 0.38500 | -2.99e-01 | -0.242000 | 8.60e-02 | 1.64e-01 | 
| Post NMDA receptor activation events | 36 | 2.09e-03 | 0.07500 | 0.38300 | 3.32e-01 | 0.190000 | 5.62e-04 | 4.88e-02 | 
| Homologous DNA Pairing and Strand Exchange | 35 | 1.13e-02 | 0.17000 | 0.38200 | -2.66e-01 | -0.275000 | 6.58e-03 | 4.97e-03 | 
| Prostacyclin signalling through prostacyclin receptor | 10 | 2.36e-01 | 0.59500 | 0.38100 | 2.21e-01 | 0.310000 | 2.26e-01 | 8.92e-02 | 
| Synthesis of PA | 15 | 1.33e-01 | 0.49100 | 0.37600 | 2.99e-01 | 0.229000 | 4.52e-02 | 1.25e-01 | 
| Meiosis | 39 | 3.51e-03 | 0.10400 | 0.37500 | -2.09e-01 | -0.311000 | 2.41e-02 | 7.85e-04 | 
| Downregulation of ERBB2 signaling | 17 | 6.90e-02 | 0.38800 | 0.37400 | -1.93e-01 | -0.320000 | 1.69e-01 | 2.22e-02 | 
| Myogenesis | 13 | 1.19e-04 | 0.03480 | 0.37200 | 2.19e-01 | -0.300000 | 1.71e-01 | 6.10e-02 | 
| Diseases associated with O-glycosylation of proteins | 17 | 1.03e-01 | 0.45400 | 0.37200 | 2.98e-01 | 0.221000 | 3.32e-02 | 1.14e-01 | 
| RNA Polymerase II Transcription Termination | 38 | 9.89e-03 | 0.15600 | 0.37100 | -2.52e-01 | -0.272000 | 7.13e-03 | 3.72e-03 | 
| Netrin-1 signaling | 24 | 1.66e-02 | 0.21200 | 0.37000 | 3.27e-01 | 0.173000 | 5.54e-03 | 1.43e-01 | 
| HDR through Single Strand Annealing (SSA) | 33 | 1.93e-02 | 0.21900 | 0.36600 | -2.41e-01 | -0.275000 | 1.68e-02 | 6.23e-03 | 
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 16 | 9.24e-02 | 0.43300 | 0.36600 | 3.12e-01 | 0.190000 | 3.06e-02 | 1.88e-01 | 
| Processing of Capped Intronless Pre-mRNA | 23 | 5.38e-02 | 0.36100 | 0.36300 | -2.16e-01 | -0.291000 | 7.26e-02 | 1.58e-02 | 
| Leading Strand Synthesis | 12 | 2.30e-01 | 0.58800 | 0.36100 | -2.23e-01 | -0.284000 | 1.81e-01 | 8.86e-02 | 
| Polymerase switching | 12 | 2.30e-01 | 0.58800 | 0.36100 | -2.23e-01 | -0.284000 | 1.81e-01 | 8.86e-02 | 
| Citric acid cycle (TCA cycle) | 18 | 1.29e-01 | 0.49100 | 0.36000 | -2.52e-01 | -0.257000 | 6.43e-02 | 5.92e-02 | 
| Hh mutants abrogate ligand secretion | 45 | 5.59e-03 | 0.11500 | 0.35900 | -2.70e-01 | -0.237000 | 1.75e-03 | 5.91e-03 | 
| Stabilization of p53 | 46 | 5.63e-03 | 0.11500 | 0.35900 | -2.49e-01 | -0.258000 | 3.55e-03 | 2.48e-03 | 
| Activation of NMDA receptors and postsynaptic events | 42 | 4.41e-03 | 0.11200 | 0.35800 | 2.94e-01 | 0.204000 | 9.91e-04 | 2.23e-02 | 
| Negative regulation of FGFR1 signaling | 17 | 1.43e-01 | 0.49100 | 0.35700 | -2.69e-01 | -0.236000 | 5.52e-02 | 9.27e-02 | 
| Negative regulation of FGFR2 signaling | 17 | 1.43e-01 | 0.49100 | 0.35700 | -2.69e-01 | -0.236000 | 5.52e-02 | 9.27e-02 | 
| Negative regulation of FGFR3 signaling | 17 | 1.43e-01 | 0.49100 | 0.35700 | -2.69e-01 | -0.236000 | 5.52e-02 | 9.27e-02 | 
| Negative regulation of FGFR4 signaling | 17 | 1.43e-01 | 0.49100 | 0.35700 | -2.69e-01 | -0.236000 | 5.52e-02 | 9.27e-02 | 
| SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 10 | 1.06e-01 | 0.45700 | 0.35600 | -3.39e-01 | -0.109000 | 6.32e-02 | 5.52e-01 | 
| Hh mutants are degraded by ERAD | 44 | 8.49e-03 | 0.14500 | 0.35100 | -2.57e-01 | -0.239000 | 3.25e-03 | 6.09e-03 | 
| Inwardly rectifying K+ channels | 11 | 2.59e-01 | 0.60300 | 0.35000 | 2.01e-01 | 0.286000 | 2.47e-01 | 1.00e-01 | 
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 14 | 2.23e-01 | 0.58100 | 0.34900 | 2.49e-01 | 0.245000 | 1.07e-01 | 1.12e-01 | 
| Class A/1 (Rhodopsin-like receptors) | 40 | 1.36e-02 | 0.19000 | 0.34800 | 2.59e-01 | 0.232000 | 4.59e-03 | 1.14e-02 | 
| Collagen degradation | 10 | 1.88e-02 | 0.21800 | 0.34500 | -2.67e-02 | 0.344000 | 8.84e-01 | 5.94e-02 | 
| Neurexins and neuroligins | 20 | 8.46e-02 | 0.42200 | 0.34500 | 2.87e-01 | 0.191000 | 2.65e-02 | 1.38e-01 | 
| Hedgehog ligand biogenesis | 48 | 6.76e-03 | 0.13200 | 0.34500 | -2.48e-01 | -0.239000 | 2.94e-03 | 4.21e-03 | 
| Synthesis of IP3 and IP4 in the cytosol | 16 | 6.05e-02 | 0.37600 | 0.34500 | 3.17e-01 | 0.134000 | 2.80e-02 | 3.53e-01 | 
| Erythropoietin activates RAS | 10 | 2.33e-02 | 0.22800 | 0.34500 | -1.34e-02 | 0.344000 | 9.42e-01 | 5.94e-02 | 
| Processive synthesis on the C-strand of the telomere | 17 | 1.67e-01 | 0.51200 | 0.34400 | -2.57e-01 | -0.228000 | 6.64e-02 | 1.04e-01 | 
| Interleukin-20 family signaling | 13 | 3.74e-02 | 0.29800 | 0.34300 | 7.01e-02 | 0.336000 | 6.62e-01 | 3.62e-02 | 
| Signaling by Erythropoietin | 18 | 1.90e-02 | 0.21800 | 0.34200 | 9.32e-02 | 0.329000 | 4.94e-01 | 1.58e-02 | 
| Adrenaline,noradrenaline inhibits insulin secretion | 12 | 1.52e-01 | 0.50900 | 0.33900 | 3.07e-01 | 0.144000 | 6.56e-02 | 3.86e-01 | 
| GPCR ligand binding | 68 | 5.74e-04 | 0.05860 | 0.33900 | 2.04e-01 | 0.271000 | 3.77e-03 | 1.15e-04 | 
| Generation of second messenger molecules | 12 | 1.20e-01 | 0.47100 | 0.33600 | 1.22e-01 | 0.313000 | 4.66e-01 | 6.06e-02 | 
| Gap-filling DNA repair synthesis and ligation in GG-NER | 23 | 9.26e-02 | 0.43300 | 0.33500 | -2.12e-01 | -0.260000 | 7.90e-02 | 3.10e-02 | 
| Purine salvage | 10 | 3.51e-01 | 0.69300 | 0.33300 | -2.63e-01 | -0.204000 | 1.50e-01 | 2.64e-01 | 
| Gap junction trafficking and regulation | 10 | 1.09e-01 | 0.46300 | 0.33200 | 3.22e-01 | 0.079900 | 7.77e-02 | 6.62e-01 | 
| Autodegradation of the E3 ubiquitin ligase COP1 | 41 | 1.95e-02 | 0.21900 | 0.33100 | -2.31e-01 | -0.237000 | 1.05e-02 | 8.68e-03 | 
| Regulation of TP53 Activity through Methylation | 16 | 2.12e-01 | 0.56800 | 0.33000 | -2.19e-01 | -0.247000 | 1.30e-01 | 8.76e-02 | 
| Cell junction organization | 21 | 7.86e-02 | 0.41000 | 0.32900 | 1.70e-01 | 0.281000 | 1.77e-01 | 2.56e-02 | 
| HDR through MMEJ (alt-NHEJ) | 11 | 3.48e-01 | 0.69100 | 0.32700 | -2.46e-01 | -0.216000 | 1.58e-01 | 2.15e-01 | 
| Nucleotide catabolism | 20 | 1.38e-01 | 0.49100 | 0.32700 | -2.05e-01 | -0.255000 | 1.13e-01 | 4.85e-02 | 
| Downregulation of ERBB2:ERBB3 signaling | 10 | 3.77e-01 | 0.71100 | 0.32500 | -2.53e-01 | -0.204000 | 1.67e-01 | 2.65e-01 | 
| Removal of the Flap Intermediate | 12 | 2.60e-01 | 0.60300 | 0.32400 | -1.75e-01 | -0.273000 | 2.95e-01 | 1.02e-01 | 
| Diseases of DNA repair | 41 | 2.19e-02 | 0.22800 | 0.32300 | -2.43e-01 | -0.214000 | 7.26e-03 | 1.80e-02 | 
| ER Quality Control Compartment (ERQC) | 18 | 1.87e-01 | 0.53400 | 0.32300 | -2.42e-01 | -0.214000 | 7.58e-02 | 1.16e-01 | 
| SARS-CoV-2 modulates host translation machinery | 38 | 2.63e-02 | 0.23500 | 0.32100 | -2.00e-01 | -0.251000 | 3.33e-02 | 7.44e-03 | 
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 10 | 4.07e-01 | 0.71500 | 0.32000 | -2.21e-01 | -0.231000 | 2.26e-01 | 2.06e-01 | 
| Spry regulation of FGF signaling | 15 | 2.52e-01 | 0.59800 | 0.32000 | -2.42e-01 | -0.209000 | 1.05e-01 | 1.62e-01 | 
| Ion transport by P-type ATPases | 27 | 6.58e-02 | 0.37900 | 0.31900 | 2.60e-01 | 0.185000 | 1.97e-02 | 9.67e-02 | 
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 15 | 2.30e-01 | 0.58800 | 0.31900 | -1.91e-01 | -0.255000 | 2.02e-01 | 8.69e-02 | 
| Deposition of new CENPA-containing nucleosomes at the centromere | 20 | 1.31e-01 | 0.49100 | 0.31500 | -1.77e-01 | -0.260000 | 1.72e-01 | 4.40e-02 | 
| Nucleosome assembly | 20 | 1.31e-01 | 0.49100 | 0.31500 | -1.77e-01 | -0.260000 | 1.72e-01 | 4.40e-02 | 
| ER-Phagosome pathway | 63 | 4.32e-03 | 0.11200 | 0.31300 | -2.10e-01 | -0.232000 | 3.92e-03 | 1.50e-03 | 
| LDL clearance | 11 | 2.49e-01 | 0.59600 | 0.31300 | -1.41e-01 | -0.279000 | 4.18e-01 | 1.09e-01 | 
| G alpha (i) signalling events | 81 | 9.18e-04 | 0.05960 | 0.31200 | 2.33e-01 | 0.208000 | 2.96e-04 | 1.25e-03 | 
| Caspase activation via extrinsic apoptotic signalling pathway | 15 | 1.70e-01 | 0.51200 | 0.31200 | -1.49e-01 | -0.274000 | 3.18e-01 | 6.64e-02 | 
| Vif-mediated degradation of APOBEC3G | 40 | 3.45e-02 | 0.28200 | 0.30900 | -2.26e-01 | -0.211000 | 1.35e-02 | 2.09e-02 | 
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 46 | 1.02e-02 | 0.15900 | 0.30700 | -2.58e-01 | -0.168000 | 2.53e-03 | 4.95e-02 | 
| Neurotransmitter receptors and postsynaptic signal transmission | 72 | 1.24e-03 | 0.06580 | 0.30600 | 2.50e-01 | 0.177000 | 2.53e-04 | 9.58e-03 | 
| FOXO-mediated transcription of cell death genes | 14 | 8.43e-02 | 0.42200 | 0.30600 | 8.35e-02 | 0.294000 | 5.89e-01 | 5.65e-02 | 
| Pre-NOTCH Processing in Golgi | 15 | 6.32e-02 | 0.37900 | 0.30600 | 2.96e-01 | 0.076900 | 4.72e-02 | 6.06e-01 | 
| Defective CFTR causes cystic fibrosis | 49 | 1.81e-02 | 0.21400 | 0.30600 | -2.13e-01 | -0.220000 | 1.00e-02 | 7.90e-03 | 
| Processing of DNA double-strand break ends | 51 | 9.03e-03 | 0.14500 | 0.30500 | -1.76e-01 | -0.249000 | 2.97e-02 | 2.15e-03 | 
| Transport of the SLBP independent Mature mRNA | 30 | 3.16e-02 | 0.26500 | 0.30400 | -2.69e-01 | -0.142000 | 1.08e-02 | 1.78e-01 | 
| Class B/2 (Secretin family receptors) | 26 | 1.79e-02 | 0.21400 | 0.30300 | 9.92e-02 | 0.286000 | 3.82e-01 | 1.15e-02 | 
| Plasma lipoprotein clearance | 21 | 1.47e-01 | 0.49800 | 0.30300 | -1.76e-01 | -0.247000 | 1.64e-01 | 5.03e-02 | 
| Peptide ligand-binding receptors | 17 | 2.57e-01 | 0.60300 | 0.30200 | 2.17e-01 | 0.210000 | 1.22e-01 | 1.34e-01 | 
| Export of Viral Ribonucleoproteins from Nucleus | 29 | 4.85e-02 | 0.34400 | 0.30100 | -2.60e-01 | -0.152000 | 1.54e-02 | 1.56e-01 | 
| Transport of the SLBP Dependant Mature mRNA | 31 | 2.10e-02 | 0.22800 | 0.30100 | -2.73e-01 | -0.127000 | 8.60e-03 | 2.23e-01 | 
| TICAM1-dependent activation of IRF3/IRF7 | 12 | 2.11e-01 | 0.56800 | 0.30100 | -2.75e-01 | -0.121000 | 9.91e-02 | 4.67e-01 | 
| Homology Directed Repair | 83 | 8.83e-04 | 0.05960 | 0.29900 | -1.81e-01 | -0.238000 | 4.53e-03 | 1.84e-04 | 
| Regulation of TP53 Activity through Phosphorylation | 74 | 1.16e-03 | 0.06480 | 0.29800 | -1.66e-01 | -0.247000 | 1.35e-02 | 2.41e-04 | 
| Diseases associated with glycosaminoglycan metabolism | 16 | 9.26e-02 | 0.43300 | 0.29800 | 2.81e-01 | 0.098500 | 5.16e-02 | 4.95e-01 | 
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 26 | 8.54e-02 | 0.42200 | 0.29800 | 2.50e-01 | 0.161000 | 2.72e-02 | 1.55e-01 | 
| Visual phototransduction | 31 | 1.07e-02 | 0.16300 | 0.29800 | 2.80e-01 | 0.100000 | 6.95e-03 | 3.34e-01 | 
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 77 | 1.13e-03 | 0.06480 | 0.29800 | -1.71e-01 | -0.243000 | 9.51e-03 | 2.29e-04 | 
| Miscellaneous transport and binding events | 13 | 1.31e-02 | 0.18600 | 0.29700 | 5.62e-02 | -0.291000 | 7.26e-01 | 6.90e-02 | 
| G alpha (z) signalling events | 22 | 7.92e-02 | 0.41000 | 0.29700 | 2.66e-01 | 0.132000 | 3.10e-02 | 2.85e-01 | 
| Chondroitin sulfate/dermatan sulfate metabolism | 24 | 1.57e-01 | 0.51200 | 0.29700 | 2.11e-01 | 0.209000 | 7.40e-02 | 7.70e-02 | 
| NGF-stimulated transcription | 25 | 9.01e-03 | 0.14500 | 0.29600 | -2.90e-01 | -0.060200 | 1.22e-02 | 6.02e-01 | 
| p53-Dependent G1 DNA Damage Response | 53 | 1.73e-02 | 0.21200 | 0.29600 | -2.06e-01 | -0.212000 | 9.68e-03 | 7.56e-03 | 
| p53-Dependent G1/S DNA damage checkpoint | 53 | 1.73e-02 | 0.21200 | 0.29600 | -2.06e-01 | -0.212000 | 9.68e-03 | 7.56e-03 | 
| Reproduction | 43 | 1.62e-02 | 0.20900 | 0.29400 | -1.53e-01 | -0.251000 | 8.21e-02 | 4.45e-03 | 
| Nuclear Pore Complex (NPC) Disassembly | 32 | 5.86e-02 | 0.37200 | 0.29300 | -2.43e-01 | -0.164000 | 1.74e-02 | 1.09e-01 | 
| Transport of Mature Transcript to Cytoplasm | 55 | 1.28e-02 | 0.18600 | 0.29300 | -2.28e-01 | -0.184000 | 3.46e-03 | 1.86e-02 | 
| SUMOylation of immune response proteins | 10 | 4.63e-01 | 0.73800 | 0.29200 | 2.21e-01 | 0.191000 | 2.26e-01 | 2.96e-01 | 
| Detoxification of Reactive Oxygen Species | 22 | 1.46e-01 | 0.49400 | 0.29200 | 1.64e-01 | 0.242000 | 1.85e-01 | 4.99e-02 | 
| Interleukin-6 signaling | 10 | 7.26e-02 | 0.39500 | 0.29000 | -2.90e-01 | 0.007680 | 1.12e-01 | 9.66e-01 | 
| Regulation of HSF1-mediated heat shock response | 63 | 8.50e-03 | 0.14500 | 0.29000 | -2.21e-01 | -0.188000 | 2.47e-03 | 1.01e-02 | 
| Retinoid metabolism and transport | 10 | 2.60e-01 | 0.60300 | 0.28800 | 2.71e-01 | 0.100000 | 1.39e-01 | 5.83e-01 | 
| Recognition of DNA damage by PCNA-containing replication complex | 26 | 7.15e-02 | 0.39200 | 0.28800 | -1.36e-01 | -0.253000 | 2.29e-01 | 2.55e-02 | 
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 39 | 5.75e-02 | 0.37200 | 0.28700 | -2.14e-01 | -0.191000 | 2.09e-02 | 3.87e-02 | 
| Transport of Mature mRNA Derived from an Intronless Transcript | 37 | 6.71e-02 | 0.38200 | 0.28600 | -2.14e-01 | -0.190000 | 2.44e-02 | 4.53e-02 | 
| Cytochrome P450 - arranged by substrate type | 14 | 3.08e-01 | 0.65200 | 0.28600 | 2.37e-01 | 0.160000 | 1.25e-01 | 2.99e-01 | 
| Ubiquitin-dependent degradation of Cyclin D | 41 | 5.27e-02 | 0.35800 | 0.28600 | -2.07e-01 | -0.198000 | 2.21e-02 | 2.86e-02 | 
| RIP-mediated NFkB activation via ZBP1 | 13 | 3.76e-01 | 0.71100 | 0.28600 | -1.80e-01 | -0.222000 | 2.61e-01 | 1.67e-01 | 
| Translesion synthesis by POLK | 15 | 2.07e-01 | 0.56200 | 0.28500 | -1.29e-01 | -0.255000 | 3.88e-01 | 8.80e-02 | 
| ZBP1(DAI) mediated induction of type I IFNs | 16 | 3.17e-01 | 0.66200 | 0.28500 | -1.92e-01 | -0.210000 | 1.84e-01 | 1.46e-01 | 
| Sensory processing of sound | 23 | 1.93e-01 | 0.53900 | 0.28400 | 1.92e-01 | 0.210000 | 1.11e-01 | 8.21e-02 | 
| Sensory processing of sound by inner hair cells of the cochlea | 23 | 1.93e-01 | 0.53900 | 0.28400 | 1.92e-01 | 0.210000 | 1.11e-01 | 8.21e-02 | 
| COPII-mediated vesicle transport | 47 | 3.33e-02 | 0.27400 | 0.28400 | -1.85e-01 | -0.215000 | 2.81e-02 | 1.08e-02 | 
| G2/M DNA damage checkpoint | 51 | 1.58e-02 | 0.20500 | 0.28300 | -1.61e-01 | -0.233000 | 4.76e-02 | 3.98e-03 | 
| G beta:gamma signalling through CDC42 | 11 | 4.62e-01 | 0.73800 | 0.28300 | 1.94e-01 | 0.205000 | 2.65e-01 | 2.39e-01 | 
| Inactivation, recovery and regulation of the phototransduction cascade | 16 | 4.26e-02 | 0.31700 | 0.28200 | 2.80e-01 | 0.035200 | 5.25e-02 | 8.08e-01 | 
| The phototransduction cascade | 16 | 4.26e-02 | 0.31700 | 0.28200 | 2.80e-01 | 0.035200 | 5.25e-02 | 8.08e-01 | 
| Condensation of Prophase Chromosomes | 12 | 1.56e-01 | 0.51200 | 0.28200 | -7.20e-02 | -0.272000 | 6.66e-01 | 1.03e-01 | 
| ISG15 antiviral mechanism | 66 | 3.86e-03 | 0.10700 | 0.28100 | -2.37e-01 | -0.152000 | 9.01e-04 | 3.33e-02 | 
| Transport of Mature mRNAs Derived from Intronless Transcripts | 38 | 6.28e-02 | 0.37900 | 0.28100 | -2.19e-01 | -0.176000 | 1.98e-02 | 6.03e-02 | 
| Sensory Perception | 61 | 4.12e-03 | 0.11200 | 0.28100 | 2.42e-01 | 0.142000 | 1.09e-03 | 5.55e-02 | 
| Antiviral mechanism by IFN-stimulated genes | 72 | 2.07e-03 | 0.07500 | 0.28100 | -2.38e-01 | -0.148000 | 4.82e-04 | 3.00e-02 | 
| N-Glycan antennae elongation | 11 | 3.95e-01 | 0.71200 | 0.28100 | 1.51e-01 | 0.236000 | 3.85e-01 | 1.75e-01 | 
| Signaling by CSF3 (G-CSF) | 23 | 2.81e-02 | 0.24500 | 0.27900 | -2.71e-01 | -0.068300 | 2.46e-02 | 5.71e-01 | 
| Metabolism of non-coding RNA | 45 | 2.15e-02 | 0.22800 | 0.27800 | -2.37e-01 | -0.145000 | 6.02e-03 | 9.29e-02 | 
| snRNP Assembly | 45 | 2.15e-02 | 0.22800 | 0.27800 | -2.37e-01 | -0.145000 | 6.02e-03 | 9.29e-02 | 
| Collagen formation | 18 | 1.11e-01 | 0.46300 | 0.27700 | 9.86e-02 | 0.259000 | 4.69e-01 | 5.70e-02 | 
| Regulation of IFNG signaling | 12 | 1.55e-02 | 0.20300 | 0.27700 | -1.09e-01 | 0.254000 | 5.13e-01 | 1.28e-01 | 
| VEGFR2 mediated cell proliferation | 16 | 4.19e-02 | 0.31600 | 0.27700 | 2.75e-01 | 0.026600 | 5.67e-02 | 8.54e-01 | 
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 21 | 2.10e-01 | 0.56600 | 0.27600 | 2.23e-01 | 0.163000 | 7.72e-02 | 1.97e-01 | 
| Aggrephagy | 19 | 2.80e-01 | 0.62300 | 0.27600 | -1.91e-01 | -0.199000 | 1.49e-01 | 1.33e-01 | 
| Cleavage of the damaged pyrimidine | 14 | 3.93e-01 | 0.71200 | 0.27600 | -1.99e-01 | -0.191000 | 1.98e-01 | 2.16e-01 | 
| Depyrimidination | 14 | 3.93e-01 | 0.71200 | 0.27600 | -1.99e-01 | -0.191000 | 1.98e-01 | 2.16e-01 | 
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 14 | 3.93e-01 | 0.71200 | 0.27600 | -1.99e-01 | -0.191000 | 1.98e-01 | 2.16e-01 | 
| Other interleukin signaling | 12 | 4.40e-01 | 0.72700 | 0.27400 | 2.10e-01 | 0.177000 | 2.08e-01 | 2.89e-01 | 
| HCMV Early Events | 48 | 2.63e-02 | 0.23500 | 0.27400 | -2.25e-01 | -0.157000 | 7.00e-03 | 6.09e-02 | 
| ABC transporter disorders | 55 | 2.43e-02 | 0.23100 | 0.27400 | -1.78e-01 | -0.208000 | 2.28e-02 | 7.59e-03 | 
| RHO GTPases Activate ROCKs | 13 | 3.71e-01 | 0.71100 | 0.27400 | -2.26e-01 | -0.155000 | 1.59e-01 | 3.32e-01 | 
| CD209 (DC-SIGN) signaling | 15 | 1.40e-01 | 0.49100 | 0.27400 | 8.46e-02 | 0.260000 | 5.71e-01 | 8.12e-02 | 
| Beta-catenin phosphorylation cascade | 15 | 2.88e-01 | 0.62700 | 0.27400 | 2.33e-01 | 0.143000 | 1.18e-01 | 3.39e-01 | 
| Carboxyterminal post-translational modifications of tubulin | 19 | 2.78e-01 | 0.62100 | 0.27300 | 1.78e-01 | 0.207000 | 1.79e-01 | 1.18e-01 | 
| Nucleotide biosynthesis | 12 | 3.97e-01 | 0.71200 | 0.27300 | 1.53e-01 | 0.226000 | 3.60e-01 | 1.75e-01 | 
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 33 | 1.06e-01 | 0.45700 | 0.27300 | -1.74e-01 | -0.210000 | 8.45e-02 | 3.67e-02 | 
| DNA Double-Strand Break Repair | 108 | 7.12e-04 | 0.05860 | 0.27200 | -1.72e-01 | -0.210000 | 2.04e-03 | 1.70e-04 | 
| APC truncation mutants have impaired AXIN binding | 12 | 4.13e-01 | 0.71700 | 0.27100 | 2.22e-01 | 0.156000 | 1.84e-01 | 3.48e-01 | 
| AXIN missense mutants destabilize the destruction complex | 12 | 4.13e-01 | 0.71700 | 0.27100 | 2.22e-01 | 0.156000 | 1.84e-01 | 3.48e-01 | 
| Signaling by AMER1 mutants | 12 | 4.13e-01 | 0.71700 | 0.27100 | 2.22e-01 | 0.156000 | 1.84e-01 | 3.48e-01 | 
| Signaling by APC mutants | 12 | 4.13e-01 | 0.71700 | 0.27100 | 2.22e-01 | 0.156000 | 1.84e-01 | 3.48e-01 | 
| Signaling by AXIN mutants | 12 | 4.13e-01 | 0.71700 | 0.27100 | 2.22e-01 | 0.156000 | 1.84e-01 | 3.48e-01 | 
| Truncations of AMER1 destabilize the destruction complex | 12 | 4.13e-01 | 0.71700 | 0.27100 | 2.22e-01 | 0.156000 | 1.84e-01 | 3.48e-01 | 
| Sensory processing of sound by outer hair cells of the cochlea | 14 | 4.05e-01 | 0.71500 | 0.27100 | 1.96e-01 | 0.188000 | 2.05e-01 | 2.24e-01 | 
| Phase I - Functionalization of compounds | 29 | 1.15e-01 | 0.46500 | 0.27100 | 1.54e-01 | 0.223000 | 1.53e-01 | 3.74e-02 | 
| ADP signalling through P2Y purinoceptor 1 | 12 | 4.32e-01 | 0.72100 | 0.27000 | 2.16e-01 | 0.163000 | 1.96e-01 | 3.27e-01 | 
| GABA receptor activation | 16 | 3.51e-01 | 0.69300 | 0.27000 | 2.03e-01 | 0.178000 | 1.59e-01 | 2.17e-01 | 
| Telomere Extension By Telomerase | 18 | 3.12e-01 | 0.65400 | 0.27000 | -1.82e-01 | -0.200000 | 1.81e-01 | 1.43e-01 | 
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 26 | 1.35e-01 | 0.49100 | 0.27000 | -2.26e-01 | -0.148000 | 4.61e-02 | 1.92e-01 | 
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 26 | 1.35e-01 | 0.49100 | 0.27000 | -2.26e-01 | -0.148000 | 4.61e-02 | 1.92e-01 | 
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 43 | 6.32e-02 | 0.37900 | 0.27000 | -1.84e-01 | -0.198000 | 3.71e-02 | 2.50e-02 | 
| EGFR downregulation | 20 | 5.74e-02 | 0.37200 | 0.26900 | -6.74e-02 | -0.261000 | 6.02e-01 | 4.36e-02 | 
| HSF1 activation | 21 | 2.65e-01 | 0.61100 | 0.26800 | -1.87e-01 | -0.192000 | 1.38e-01 | 1.27e-01 | 
| Synthesis of very long-chain fatty acyl-CoAs | 10 | 6.41e-02 | 0.37900 | 0.26800 | -5.27e-02 | 0.263000 | 7.73e-01 | 1.50e-01 | 
| RUNX3 regulates p14-ARF | 10 | 5.24e-01 | 0.77400 | 0.26800 | -2.03e-01 | -0.174000 | 2.66e-01 | 3.40e-01 | 
| RAC3 GTPase cycle | 54 | 1.87e-03 | 0.07500 | 0.26700 | 9.12e-02 | 0.251000 | 2.47e-01 | 1.44e-03 | 
| Regulation of TP53 Degradation | 33 | 8.26e-02 | 0.41800 | 0.26600 | -1.44e-01 | -0.224000 | 1.53e-01 | 2.61e-02 | 
| Regulation of TP53 Expression and Degradation | 33 | 8.26e-02 | 0.41800 | 0.26600 | -1.44e-01 | -0.224000 | 1.53e-01 | 2.61e-02 | 
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 43 | 5.84e-02 | 0.37200 | 0.26600 | -2.09e-01 | -0.165000 | 1.79e-02 | 6.21e-02 | 
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 23 | 1.81e-01 | 0.52300 | 0.26500 | -1.45e-01 | -0.222000 | 2.30e-01 | 6.55e-02 | 
| Neuronal System | 124 | 3.84e-04 | 0.05670 | 0.26500 | 2.04e-01 | 0.169000 | 9.22e-05 | 1.22e-03 | 
| Termination of translesion DNA synthesis | 27 | 1.92e-01 | 0.53900 | 0.26400 | -1.86e-01 | -0.188000 | 9.54e-02 | 9.09e-02 | 
| Transmission across Chemical Synapses | 91 | 3.29e-03 | 0.10100 | 0.26400 | 2.02e-01 | 0.169000 | 8.84e-04 | 5.31e-03 | 
| NEP/NS2 Interacts with the Cellular Export Machinery | 28 | 8.64e-02 | 0.42200 | 0.26400 | -2.34e-01 | -0.122000 | 3.23e-02 | 2.65e-01 | 
| Lagging Strand Synthesis | 17 | 2.74e-01 | 0.61700 | 0.26400 | -1.39e-01 | -0.224000 | 3.20e-01 | 1.10e-01 | 
| mRNA Splicing - Major Pathway | 130 | 2.07e-04 | 0.04660 | 0.26400 | -1.61e-01 | -0.209000 | 1.64e-03 | 4.07e-05 | 
| Attenuation phase | 19 | 3.14e-01 | 0.65700 | 0.26300 | -1.90e-01 | -0.182000 | 1.51e-01 | 1.69e-01 | 
| AKT phosphorylates targets in the cytosol | 13 | 2.48e-01 | 0.59600 | 0.26300 | -9.72e-02 | -0.245000 | 5.44e-01 | 1.26e-01 | 
| STING mediated induction of host immune responses | 10 | 2.99e-01 | 0.63700 | 0.26300 | 8.17e-02 | 0.250000 | 6.55e-01 | 1.71e-01 | 
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models | 20 | 1.63e-01 | 0.51200 | 0.26300 | 2.36e-01 | 0.116000 | 6.82e-02 | 3.69e-01 | 
| Neurodegenerative Diseases | 20 | 1.63e-01 | 0.51200 | 0.26300 | 2.36e-01 | 0.116000 | 6.82e-02 | 3.69e-01 | 
| RUNX2 regulates osteoblast differentiation | 12 | 1.61e-01 | 0.51200 | 0.26200 | 4.93e-02 | 0.258000 | 7.68e-01 | 1.23e-01 | 
| Thrombin signalling through proteinase activated receptors (PARs) | 16 | 2.02e-01 | 0.55000 | 0.26200 | 2.41e-01 | 0.103000 | 9.58e-02 | 4.74e-01 | 
| Depolymerisation of the Nuclear Lamina | 11 | 2.95e-01 | 0.63200 | 0.26000 | 2.45e-01 | 0.088800 | 1.60e-01 | 6.10e-01 | 
| Vpu mediated degradation of CD4 | 40 | 8.08e-02 | 0.41600 | 0.26000 | -2.04e-01 | -0.161000 | 2.59e-02 | 7.78e-02 | 
| Methylation | 10 | 5.54e-01 | 0.78700 | 0.26000 | -1.83e-01 | -0.184000 | 3.17e-01 | 3.13e-01 | 
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 10 | 3.94e-01 | 0.71200 | 0.25900 | -1.08e-01 | -0.235000 | 5.55e-01 | 1.98e-01 | 
| alpha-linolenic acid (ALA) metabolism | 10 | 3.94e-01 | 0.71200 | 0.25900 | -1.08e-01 | -0.235000 | 5.55e-01 | 1.98e-01 | 
| The role of GTSE1 in G2/M progression after G2 checkpoint | 49 | 5.64e-02 | 0.37200 | 0.25800 | -1.75e-01 | -0.190000 | 3.45e-02 | 2.17e-02 | 
| Processing of Capped Intron-Containing Pre-mRNA | 177 | 3.41e-05 | 0.01330 | 0.25800 | -1.72e-01 | -0.192000 | 8.20e-05 | 1.21e-05 | 
| Insulin processing | 15 | 3.11e-01 | 0.65400 | 0.25700 | 2.24e-01 | 0.127000 | 1.34e-01 | 3.95e-01 | 
| Resolution of Abasic Sites (AP sites) | 32 | 1.57e-01 | 0.51200 | 0.25600 | -1.71e-01 | -0.190000 | 9.35e-02 | 6.35e-02 | 
| Regulation of mRNA stability by proteins that bind AU-rich elements | 72 | 1.45e-02 | 0.19800 | 0.25500 | -1.63e-01 | -0.195000 | 1.67e-02 | 4.22e-03 | 
| DARPP-32 events | 18 | 8.89e-02 | 0.43300 | 0.25500 | 5.70e-02 | 0.248000 | 6.76e-01 | 6.84e-02 | 
| G alpha (q) signalling events | 67 | 5.84e-03 | 0.11800 | 0.25400 | 2.22e-01 | 0.124000 | 1.70e-03 | 7.99e-02 | 
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 49 | 5.03e-02 | 0.35200 | 0.25300 | -2.02e-01 | -0.154000 | 1.48e-02 | 6.30e-02 | 
| Regulation of FZD by ubiquitination | 12 | 4.17e-01 | 0.71800 | 0.25300 | 1.29e-01 | 0.218000 | 4.40e-01 | 1.92e-01 | 
| SCF(Skp2)-mediated degradation of p27/p21 | 49 | 5.81e-02 | 0.37200 | 0.25300 | -1.94e-01 | -0.162000 | 1.88e-02 | 5.07e-02 | 
| Antigen processing-Cross presentation | 68 | 2.24e-02 | 0.22800 | 0.25300 | -1.74e-01 | -0.183000 | 1.32e-02 | 9.16e-03 | 
| G1/S DNA Damage Checkpoints | 55 | 4.69e-02 | 0.33800 | 0.25200 | -1.75e-01 | -0.181000 | 2.47e-02 | 2.02e-02 | 
| COPI-mediated anterograde transport | 65 | 2.73e-02 | 0.24000 | 0.25100 | -1.72e-01 | -0.184000 | 1.69e-02 | 1.06e-02 | 
| E3 ubiquitin ligases ubiquitinate target proteins | 40 | 6.97e-02 | 0.39000 | 0.25100 | -2.10e-01 | -0.136000 | 2.15e-02 | 1.36e-01 | 
| Glucagon-type ligand receptors | 12 | 4.23e-01 | 0.71800 | 0.25100 | 1.27e-01 | 0.216000 | 4.45e-01 | 1.96e-01 | 
| Interleukin-6 family signaling | 13 | 6.09e-02 | 0.37600 | 0.25000 | -2.49e-01 | 0.025800 | 1.20e-01 | 8.72e-01 | 
| Platelet calcium homeostasis | 16 | 2.45e-01 | 0.59600 | 0.24900 | 2.27e-01 | 0.102000 | 1.16e-01 | 4.81e-01 | 
| PRC2 methylates histones and DNA | 11 | 5.50e-01 | 0.78600 | 0.24800 | -1.80e-01 | -0.171000 | 3.01e-01 | 3.26e-01 | 
| mRNA decay by 3’ to 5’ exoribonuclease | 14 | 2.74e-01 | 0.61700 | 0.24800 | -9.45e-02 | -0.229000 | 5.41e-01 | 1.38e-01 | 
| Signaling by Activin | 11 | 3.26e-02 | 0.27100 | 0.24800 | -1.94e-01 | 0.154000 | 2.66e-01 | 3.76e-01 | 
| ROS and RNS production in phagocytes | 22 | 2.91e-01 | 0.62700 | 0.24700 | 1.57e-01 | 0.191000 | 2.02e-01 | 1.21e-01 | 
| CaM pathway | 17 | 2.02e-01 | 0.55000 | 0.24700 | 2.29e-01 | 0.090900 | 1.02e-01 | 5.16e-01 | 
| Calmodulin induced events | 17 | 2.02e-01 | 0.55000 | 0.24700 | 2.29e-01 | 0.090900 | 1.02e-01 | 5.16e-01 | 
| InlB-mediated entry of Listeria monocytogenes into host cell | 11 | 5.56e-01 | 0.78700 | 0.24700 | -1.75e-01 | -0.174000 | 3.16e-01 | 3.18e-01 | 
| PCNA-Dependent Long Patch Base Excision Repair | 18 | 2.91e-01 | 0.62700 | 0.24600 | -1.26e-01 | -0.212000 | 3.54e-01 | 1.20e-01 | 
| Regulation of ornithine decarboxylase (ODC) | 40 | 1.18e-01 | 0.46600 | 0.24600 | -1.65e-01 | -0.182000 | 7.11e-02 | 4.66e-02 | 
| Degradation of GLI1 by the proteasome | 48 | 6.48e-02 | 0.37900 | 0.24600 | -1.95e-01 | -0.150000 | 1.98e-02 | 7.31e-02 | 
| Ca-dependent events | 18 | 1.92e-01 | 0.53900 | 0.24500 | 2.27e-01 | 0.092100 | 9.49e-02 | 4.99e-01 | 
| Bile acid and bile salt metabolism | 13 | 2.73e-01 | 0.61700 | 0.24400 | 2.30e-01 | 0.080800 | 1.50e-01 | 6.14e-01 | 
| Molecules associated with elastic fibres | 10 | 2.01e-01 | 0.55000 | 0.24300 | -1.68e-02 | -0.243000 | 9.27e-01 | 1.84e-01 | 
| Integrin signaling | 14 | 1.67e-01 | 0.51200 | 0.24200 | -4.75e-02 | -0.237000 | 7.59e-01 | 1.24e-01 | 
| Platelet Aggregation (Plug Formation) | 14 | 1.67e-01 | 0.51200 | 0.24200 | -4.75e-02 | -0.237000 | 7.59e-01 | 1.24e-01 | 
| Platelet homeostasis | 44 | 1.03e-01 | 0.45400 | 0.24200 | 1.65e-01 | 0.177000 | 5.93e-02 | 4.19e-02 | 
| Integrin cell surface interactions | 22 | 7.44e-02 | 0.40100 | 0.24200 | 2.35e-01 | 0.057100 | 5.68e-02 | 6.43e-01 | 
| Inactivation of CSF3 (G-CSF) signaling | 18 | 5.42e-02 | 0.36200 | 0.24200 | -2.41e-01 | -0.012700 | 7.65e-02 | 9.26e-01 | 
| Base Excision Repair | 39 | 1.37e-01 | 0.49100 | 0.24100 | -1.73e-01 | -0.168000 | 6.21e-02 | 6.92e-02 | 
| Vpr-mediated nuclear import of PICs | 30 | 1.63e-01 | 0.51200 | 0.24100 | -2.01e-01 | -0.134000 | 5.72e-02 | 2.05e-01 | 
| MicroRNA (miRNA) biogenesis | 18 | 3.97e-01 | 0.71200 | 0.24100 | -1.63e-01 | -0.178000 | 2.32e-01 | 1.92e-01 | 
| Signaling by FGFR3 | 24 | 2.19e-01 | 0.57400 | 0.24100 | -2.04e-01 | -0.127000 | 8.33e-02 | 2.81e-01 | 
| Signaling by FGFR4 | 24 | 2.19e-01 | 0.57400 | 0.24100 | -2.04e-01 | -0.127000 | 8.33e-02 | 2.81e-01 | 
| G-protein beta:gamma signalling | 18 | 2.48e-01 | 0.59600 | 0.24100 | 2.17e-01 | 0.105000 | 1.12e-01 | 4.43e-01 | 
| Meiotic synapsis | 22 | 2.35e-01 | 0.59400 | 0.24000 | -1.22e-01 | -0.207000 | 3.21e-01 | 9.30e-02 | 
| Ca2+ pathway | 34 | 1.17e-01 | 0.46600 | 0.24000 | 2.04e-01 | 0.126000 | 3.98e-02 | 2.03e-01 | 
| Lysosome Vesicle Biogenesis | 24 | 1.71e-01 | 0.51200 | 0.23900 | 2.13e-01 | 0.108000 | 7.07e-02 | 3.62e-01 | 
| mRNA Splicing | 138 | 5.60e-04 | 0.05860 | 0.23900 | -1.43e-01 | -0.191000 | 3.86e-03 | 1.12e-04 | 
| DNA Damage Bypass | 40 | 8.58e-02 | 0.42200 | 0.23900 | -1.28e-01 | -0.202000 | 1.63e-01 | 2.75e-02 | 
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 31 | 6.70e-02 | 0.38200 | 0.23800 | 8.83e-02 | 0.221000 | 3.95e-01 | 3.31e-02 | 
| PKMTs methylate histone lysines | 23 | 2.42e-01 | 0.59600 | 0.23800 | 1.27e-01 | 0.202000 | 2.94e-01 | 9.41e-02 | 
| CTNNB1 S33 mutants aren’t phosphorylated | 13 | 3.97e-01 | 0.71200 | 0.23800 | 2.11e-01 | 0.110000 | 1.88e-01 | 4.91e-01 | 
| CTNNB1 S37 mutants aren’t phosphorylated | 13 | 3.97e-01 | 0.71200 | 0.23800 | 2.11e-01 | 0.110000 | 1.88e-01 | 4.91e-01 | 
| CTNNB1 S45 mutants aren’t phosphorylated | 13 | 3.97e-01 | 0.71200 | 0.23800 | 2.11e-01 | 0.110000 | 1.88e-01 | 4.91e-01 | 
| CTNNB1 T41 mutants aren’t phosphorylated | 13 | 3.97e-01 | 0.71200 | 0.23800 | 2.11e-01 | 0.110000 | 1.88e-01 | 4.91e-01 | 
| Signaling by CTNNB1 phospho-site mutants | 13 | 3.97e-01 | 0.71200 | 0.23800 | 2.11e-01 | 0.110000 | 1.88e-01 | 4.91e-01 | 
| Signaling by GSK3beta mutants | 13 | 3.97e-01 | 0.71200 | 0.23800 | 2.11e-01 | 0.110000 | 1.88e-01 | 4.91e-01 | 
| Uptake and actions of bacterial toxins | 18 | 3.65e-01 | 0.70700 | 0.23700 | 1.93e-01 | 0.137000 | 1.56e-01 | 3.13e-01 | 
| mRNA decay by 5’ to 3’ exoribonuclease | 14 | 3.83e-01 | 0.71200 | 0.23700 | -2.08e-01 | -0.113000 | 1.77e-01 | 4.64e-01 | 
| Cellular response to heat stress | 76 | 2.27e-02 | 0.22800 | 0.23700 | -1.77e-01 | -0.157000 | 7.63e-03 | 1.80e-02 | 
| G beta:gamma signalling through PI3Kgamma | 14 | 4.97e-01 | 0.75800 | 0.23700 | 1.77e-01 | 0.158000 | 2.52e-01 | 3.06e-01 | 
| ADP signalling through P2Y purinoceptor 12 | 11 | 5.82e-01 | 0.79800 | 0.23700 | 1.66e-01 | 0.169000 | 3.41e-01 | 3.31e-01 | 
| Translesion synthesis by REV1 | 14 | 2.91e-01 | 0.62700 | 0.23600 | -8.47e-02 | -0.221000 | 5.83e-01 | 1.53e-01 | 
| Transport of Ribonucleoproteins into the Host Nucleus | 28 | 1.95e-01 | 0.54000 | 0.23600 | -1.97e-01 | -0.130000 | 7.13e-02 | 2.33e-01 | 
| Resolution of Sister Chromatid Cohesion | 88 | 8.88e-03 | 0.14500 | 0.23600 | -1.41e-01 | -0.190000 | 2.29e-02 | 2.14e-03 | 
| O-linked glycosylation | 36 | 1.04e-01 | 0.45600 | 0.23600 | 2.03e-01 | 0.121000 | 3.56e-02 | 2.10e-01 | 
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 41 | 1.36e-01 | 0.49100 | 0.23600 | -1.69e-01 | -0.164000 | 6.09e-02 | 6.98e-02 | 
| p53-Independent DNA Damage Response | 41 | 1.36e-01 | 0.49100 | 0.23600 | -1.69e-01 | -0.164000 | 6.09e-02 | 6.98e-02 | 
| p53-Independent G1/S DNA damage checkpoint | 41 | 1.36e-01 | 0.49100 | 0.23600 | -1.69e-01 | -0.164000 | 6.09e-02 | 6.98e-02 | 
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 20 | 3.11e-01 | 0.65400 | 0.23400 | -1.27e-01 | -0.197000 | 3.25e-01 | 1.28e-01 | 
| Negative regulation of NOTCH4 signaling | 45 | 1.17e-01 | 0.46600 | 0.23200 | -1.72e-01 | -0.156000 | 4.67e-02 | 7.00e-02 | 
| Triglyceride catabolism | 11 | 5.62e-01 | 0.78700 | 0.23200 | 1.87e-01 | 0.137000 | 2.83e-01 | 4.30e-01 | 
| Interactions of Vpr with host cellular proteins | 31 | 1.79e-01 | 0.51900 | 0.23100 | -1.92e-01 | -0.128000 | 6.39e-02 | 2.18e-01 | 
| Chromosome Maintenance | 71 | 2.70e-02 | 0.23900 | 0.23000 | -1.38e-01 | -0.185000 | 4.51e-02 | 7.28e-03 | 
| NOD1/2 Signaling Pathway | 22 | 7.89e-02 | 0.41000 | 0.23000 | -4.51e-02 | -0.226000 | 7.15e-01 | 6.72e-02 | 
| Inhibition of DNA recombination at telomere | 18 | 4.06e-01 | 0.71500 | 0.23000 | -1.40e-01 | -0.182000 | 3.04e-01 | 1.81e-01 | 
| Nuclear Events (kinase and transcription factor activation) | 42 | 2.61e-02 | 0.23500 | 0.22900 | -2.16e-01 | -0.077100 | 1.56e-02 | 3.88e-01 | 
| Viral Messenger RNA Synthesis | 39 | 1.62e-01 | 0.51200 | 0.22900 | -1.71e-01 | -0.153000 | 6.51e-02 | 9.87e-02 | 
| Signaling by FGFR2 | 47 | 7.85e-02 | 0.41000 | 0.22900 | -1.90e-01 | -0.128000 | 2.42e-02 | 1.29e-01 | 
| DNA Double Strand Break Response | 34 | 1.73e-01 | 0.51400 | 0.22900 | -1.34e-01 | -0.186000 | 1.76e-01 | 6.13e-02 | 
| Degradation of DVL | 45 | 1.26e-01 | 0.48900 | 0.22900 | -1.56e-01 | -0.167000 | 7.02e-02 | 5.25e-02 | 
| Complex I biogenesis | 38 | 1.75e-01 | 0.51400 | 0.22900 | -1.65e-01 | -0.158000 | 7.86e-02 | 9.15e-02 | 
| Heparan sulfate/heparin (HS-GAG) metabolism | 22 | 2.89e-01 | 0.62700 | 0.22900 | 1.93e-01 | 0.122000 | 1.17e-01 | 3.20e-01 | 
| G2/M Checkpoints | 106 | 7.99e-03 | 0.14400 | 0.22800 | -1.53e-01 | -0.169000 | 6.72e-03 | 2.77e-03 | 
| NS1 Mediated Effects on Host Pathways | 36 | 1.90e-01 | 0.53700 | 0.22700 | -1.71e-01 | -0.150000 | 7.65e-02 | 1.19e-01 | 
| Degradation of GLI2 by the proteasome | 47 | 1.16e-01 | 0.46500 | 0.22700 | -1.70e-01 | -0.151000 | 4.44e-02 | 7.35e-02 | 
| GLI3 is processed to GLI3R by the proteasome | 47 | 1.16e-01 | 0.46500 | 0.22700 | -1.70e-01 | -0.151000 | 4.44e-02 | 7.35e-02 | 
| Formation of the ternary complex, and subsequently, the 43S complex | 39 | 2.60e-02 | 0.23500 | 0.22700 | -6.55e-02 | -0.217000 | 4.80e-01 | 1.91e-02 | 
| Signaling by KIT in disease | 16 | 1.27e-01 | 0.48900 | 0.22600 | 2.53e-02 | 0.225000 | 8.61e-01 | 1.20e-01 | 
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 16 | 1.27e-01 | 0.48900 | 0.22600 | 2.53e-02 | 0.225000 | 8.61e-01 | 1.20e-01 | 
| COPI-dependent Golgi-to-ER retrograde traffic | 62 | 5.20e-02 | 0.35600 | 0.22600 | -1.78e-01 | -0.139000 | 1.56e-02 | 5.94e-02 | 
| Regulation of pyruvate dehydrogenase (PDH) complex | 10 | 2.18e-01 | 0.57400 | 0.22500 | -5.70e-04 | 0.225000 | 9.98e-01 | 2.18e-01 | 
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 74 | 3.52e-02 | 0.28400 | 0.22500 | -1.71e-01 | -0.146000 | 1.13e-02 | 3.03e-02 | 
| Constitutive Signaling by AKT1 E17K in Cancer | 23 | 2.41e-01 | 0.59600 | 0.22400 | -1.06e-01 | -0.198000 | 3.78e-01 | 1.01e-01 | 
| Zinc transporters | 11 | 3.94e-01 | 0.71200 | 0.22400 | -2.12e-01 | -0.073500 | 2.24e-01 | 6.73e-01 | 
| ER to Golgi Anterograde Transport | 99 | 1.30e-02 | 0.18600 | 0.22300 | -1.50e-01 | -0.165000 | 9.98e-03 | 4.62e-03 | 
| Extension of Telomeres | 40 | 1.72e-01 | 0.51400 | 0.22300 | -1.50e-01 | -0.165000 | 1.00e-01 | 7.17e-02 | 
| PLC beta mediated events | 24 | 2.32e-02 | 0.22800 | 0.22300 | 2.23e-01 | -0.008600 | 5.92e-02 | 9.42e-01 | 
| Metabolism of fat-soluble vitamins | 12 | 3.63e-01 | 0.70500 | 0.22100 | 2.10e-01 | 0.070400 | 2.08e-01 | 6.73e-01 | 
| Recycling pathway of L1 | 15 | 2.43e-01 | 0.59600 | 0.22100 | 2.13e-01 | 0.057900 | 1.52e-01 | 6.98e-01 | 
| Nuclear import of Rev protein | 29 | 1.31e-01 | 0.49100 | 0.22100 | -2.02e-01 | -0.088200 | 5.96e-02 | 4.11e-01 | 
| RAC2 GTPase cycle | 52 | 3.23e-02 | 0.26900 | 0.22100 | 9.40e-02 | 0.199000 | 2.42e-01 | 1.29e-02 | 
| Nicotinamide salvaging | 10 | 5.15e-01 | 0.77300 | 0.22000 | 9.39e-02 | 0.199000 | 6.07e-01 | 2.75e-01 | 
| Sema4D induced cell migration and growth-cone collapse | 11 | 1.39e-01 | 0.49100 | 0.22000 | -2.17e-01 | 0.036700 | 2.13e-01 | 8.33e-01 | 
| BBSome-mediated cargo-targeting to cilium | 16 | 4.63e-01 | 0.73800 | 0.22000 | -1.28e-01 | -0.179000 | 3.76e-01 | 2.15e-01 | 
| Telomere C-strand (Lagging Strand) Synthesis | 27 | 3.20e-01 | 0.66400 | 0.21900 | -1.57e-01 | -0.154000 | 1.59e-01 | 1.67e-01 | 
| Separation of Sister Chromatids | 136 | 2.72e-03 | 0.08590 | 0.21900 | -1.40e-01 | -0.169000 | 5.03e-03 | 7.02e-04 | 
| Mitotic Prometaphase | 147 | 1.62e-03 | 0.07500 | 0.21900 | -1.37e-01 | -0.170000 | 4.24e-03 | 3.83e-04 | 
| tRNA processing in the nucleus | 52 | 1.10e-01 | 0.46300 | 0.21900 | -1.63e-01 | -0.146000 | 4.25e-02 | 6.90e-02 | 
| DAG and IP3 signaling | 23 | 1.09e-01 | 0.46300 | 0.21900 | 2.12e-01 | 0.052100 | 7.82e-02 | 6.65e-01 | 
| Translation initiation complex formation | 45 | 3.52e-02 | 0.28400 | 0.21900 | -7.95e-02 | -0.204000 | 3.57e-01 | 1.82e-02 | 
| Activation of GABAB receptors | 15 | 5.23e-01 | 0.77400 | 0.21800 | 1.67e-01 | 0.141000 | 2.64e-01 | 3.45e-01 | 
| GABA B receptor activation | 15 | 5.23e-01 | 0.77400 | 0.21800 | 1.67e-01 | 0.141000 | 2.64e-01 | 3.45e-01 | 
| Glutamate Neurotransmitter Release Cycle | 10 | 9.22e-02 | 0.43300 | 0.21800 | -1.27e-01 | 0.177000 | 4.85e-01 | 3.33e-01 | 
| Respiratory electron transport | 73 | 4.53e-02 | 0.33300 | 0.21800 | -1.64e-01 | -0.143000 | 1.53e-02 | 3.48e-02 | 
| SUMOylation of ubiquitinylation proteins | 35 | 2.29e-01 | 0.58800 | 0.21800 | -1.63e-01 | -0.144000 | 9.57e-02 | 1.40e-01 | 
| Oncogenic MAPK signaling | 54 | 2.94e-02 | 0.25100 | 0.21800 | 1.98e-01 | 0.091100 | 1.22e-02 | 2.48e-01 | 
| Downstream signaling of activated FGFR1 | 11 | 2.45e-01 | 0.59600 | 0.21700 | -2.17e-01 | -0.015100 | 2.13e-01 | 9.31e-01 | 
| Downstream signaling of activated FGFR2 | 11 | 2.45e-01 | 0.59600 | 0.21700 | -2.17e-01 | -0.015100 | 2.13e-01 | 9.31e-01 | 
| Downstream signaling of activated FGFR3 | 11 | 2.45e-01 | 0.59600 | 0.21700 | -2.17e-01 | -0.015100 | 2.13e-01 | 9.31e-01 | 
| Downstream signaling of activated FGFR4 | 11 | 2.45e-01 | 0.59600 | 0.21700 | -2.17e-01 | -0.015100 | 2.13e-01 | 9.31e-01 | 
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 43 | 1.58e-01 | 0.51200 | 0.21700 | -1.67e-01 | -0.140000 | 5.91e-02 | 1.14e-01 | 
| MAPK targets/ Nuclear events mediated by MAP kinases | 22 | 1.69e-01 | 0.51200 | 0.21700 | -2.06e-01 | -0.069600 | 9.49e-02 | 5.72e-01 | 
| Interleukin-35 Signalling | 11 | 5.17e-01 | 0.77300 | 0.21700 | 9.87e-02 | 0.193000 | 5.71e-01 | 2.68e-01 | 
| Regulation of RUNX1 Expression and Activity | 14 | 5.23e-01 | 0.77400 | 0.21600 | -1.26e-01 | -0.176000 | 4.13e-01 | 2.55e-01 | 
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 16 | 5.06e-01 | 0.76600 | 0.21600 | -1.38e-01 | -0.166000 | 3.38e-01 | 2.51e-01 | 
| Base-Excision Repair, AP Site Formation | 16 | 3.89e-01 | 0.71200 | 0.21600 | -1.92e-01 | -0.099200 | 1.85e-01 | 4.92e-01 | 
| Signaling by Retinoic Acid | 17 | 2.82e-01 | 0.62400 | 0.21500 | 7.48e-02 | 0.201000 | 5.94e-01 | 1.51e-01 | 
| Hyaluronan metabolism | 10 | 2.94e-01 | 0.63200 | 0.21500 | -1.76e-02 | -0.214000 | 9.23e-01 | 2.41e-01 | 
| Metalloprotease DUBs | 16 | 5.25e-01 | 0.77400 | 0.21400 | -1.54e-01 | -0.149000 | 2.88e-01 | 3.01e-01 | 
| RAF activation | 28 | 3.25e-01 | 0.66800 | 0.21300 | 1.45e-01 | 0.156000 | 1.84e-01 | 1.53e-01 | 
| Heme signaling | 25 | 3.68e-01 | 0.71000 | 0.21300 | 1.46e-01 | 0.155000 | 2.07e-01 | 1.79e-01 | 
| NIK–>noncanonical NF-kB signaling | 46 | 1.63e-01 | 0.51200 | 0.21200 | -1.55e-01 | -0.145000 | 6.94e-02 | 9.02e-02 | 
| Telomere Maintenance | 53 | 1.13e-01 | 0.46300 | 0.21100 | -1.33e-01 | -0.165000 | 9.47e-02 | 3.85e-02 | 
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 12 | 5.34e-01 | 0.77400 | 0.21100 | -1.05e-01 | -0.183000 | 5.30e-01 | 2.71e-01 | 
| Neurotransmitter release cycle | 17 | 8.48e-02 | 0.42200 | 0.21100 | -1.35e-02 | 0.210000 | 9.23e-01 | 1.34e-01 | 
| Defective pyroptosis | 10 | 6.67e-01 | 0.85000 | 0.21100 | -1.35e-01 | -0.162000 | 4.61e-01 | 3.75e-01 | 
| TBC/RABGAPs | 39 | 1.57e-01 | 0.51200 | 0.21000 | -1.13e-01 | -0.177000 | 2.21e-01 | 5.56e-02 | 
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 33 | 2.37e-01 | 0.59500 | 0.21000 | -1.22e-01 | -0.171000 | 2.25e-01 | 8.96e-02 | 
| Purine ribonucleoside monophosphate biosynthesis | 10 | 5.53e-01 | 0.78700 | 0.21000 | 9.09e-02 | 0.189000 | 6.19e-01 | 3.00e-01 | 
| RHO GTPases Activate NADPH Oxidases | 14 | 1.66e-01 | 0.51200 | 0.21000 | 2.10e-01 | 0.003920 | 1.75e-01 | 9.80e-01 | 
| Signaling by PDGFR in disease | 15 | 1.16e-01 | 0.46500 | 0.20800 | -1.56e-02 | 0.208000 | 9.17e-01 | 1.64e-01 | 
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 16 | 4.70e-01 | 0.73800 | 0.20800 | -1.10e-01 | -0.176000 | 4.45e-01 | 2.22e-01 | 
| Metabolism of folate and pterines | 11 | 6.58e-01 | 0.84600 | 0.20800 | -1.52e-01 | -0.142000 | 3.83e-01 | 4.16e-01 | 
| SARS-CoV-2-host interactions | 142 | 4.76e-03 | 0.11200 | 0.20800 | -1.53e-01 | -0.140000 | 1.71e-03 | 4.06e-03 | 
| Processive synthesis on the lagging strand | 13 | 4.60e-01 | 0.73800 | 0.20700 | -8.67e-02 | -0.188000 | 5.88e-01 | 2.40e-01 | 
| Muscle contraction | 63 | 2.18e-02 | 0.22800 | 0.20700 | 1.89e-01 | 0.084400 | 9.47e-03 | 2.47e-01 | 
| Cell Cycle Checkpoints | 208 | 3.88e-04 | 0.05670 | 0.20700 | -1.36e-01 | -0.156000 | 7.77e-04 | 1.12e-04 | 
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 44 | 5.11e-02 | 0.35400 | 0.20700 | 1.93e-01 | 0.074100 | 2.66e-02 | 3.95e-01 | 
| HATs acetylate histones | 53 | 1.32e-01 | 0.49100 | 0.20700 | -1.57e-01 | -0.135000 | 4.91e-02 | 9.02e-02 | 
| Polymerase switching on the C-strand of the telomere | 20 | 4.71e-01 | 0.73800 | 0.20600 | -1.39e-01 | -0.152000 | 2.82e-01 | 2.39e-01 | 
| Opioid Signalling | 49 | 1.14e-01 | 0.46300 | 0.20600 | 1.72e-01 | 0.114000 | 3.75e-02 | 1.70e-01 | 
| RHO GTPases Activate Formins | 97 | 1.52e-02 | 0.20200 | 0.20600 | -1.16e-01 | -0.170000 | 4.92e-02 | 3.84e-03 | 
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | 31 | 2.75e-01 | 0.61700 | 0.20600 | -1.20e-01 | -0.167000 | 2.46e-01 | 1.08e-01 | 
| Regulation of innate immune responses to cytosolic DNA | 11 | 4.86e-01 | 0.74900 | 0.20600 | -1.91e-01 | -0.075600 | 2.72e-01 | 6.64e-01 | 
| Infection with Mycobacterium tuberculosis | 20 | 4.73e-01 | 0.73800 | 0.20600 | -1.51e-01 | -0.140000 | 2.42e-01 | 2.80e-01 | 
| HSF1-dependent transactivation | 25 | 3.87e-01 | 0.71200 | 0.20600 | -1.35e-01 | -0.155000 | 2.43e-01 | 1.79e-01 | 
| Deadenylation of mRNA | 22 | 7.18e-02 | 0.39200 | 0.20600 | -2.05e-01 | -0.008000 | 9.55e-02 | 9.48e-01 | 
| SUMOylation of RNA binding proteins | 40 | 1.65e-01 | 0.51200 | 0.20400 | -1.73e-01 | -0.108000 | 5.92e-02 | 2.37e-01 | 
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 79 | 3.84e-02 | 0.29800 | 0.20400 | -1.17e-01 | -0.167000 | 7.23e-02 | 1.07e-02 | 
| Amplification of signal from the kinetochores | 79 | 3.84e-02 | 0.29800 | 0.20400 | -1.17e-01 | -0.167000 | 7.23e-02 | 1.07e-02 | 
| Transcriptional regulation by small RNAs | 41 | 1.66e-01 | 0.51200 | 0.20300 | -1.71e-01 | -0.111000 | 5.91e-02 | 2.20e-01 | 
| EML4 and NUDC in mitotic spindle formation | 83 | 3.83e-02 | 0.29800 | 0.20300 | -1.22e-01 | -0.162000 | 5.57e-02 | 1.08e-02 | 
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 46 | 7.05e-02 | 0.39100 | 0.20300 | -8.35e-02 | -0.185000 | 3.28e-01 | 3.04e-02 | 
| Host Interactions of HIV factors | 100 | 8.75e-03 | 0.14500 | 0.20300 | -1.76e-01 | -0.101000 | 2.47e-03 | 8.16e-02 | 
| Thromboxane signalling through TP receptor | 11 | 5.77e-01 | 0.79500 | 0.20300 | 1.78e-01 | 0.096700 | 3.07e-01 | 5.79e-01 | 
| Deadenylation-dependent mRNA decay | 50 | 9.11e-02 | 0.43300 | 0.20200 | -1.76e-01 | -0.099700 | 3.18e-02 | 2.23e-01 | 
| Calnexin/calreticulin cycle | 23 | 4.25e-01 | 0.71800 | 0.20200 | -1.29e-01 | -0.155000 | 2.85e-01 | 1.97e-01 | 
| Disorders of Developmental Biology | 10 | 4.42e-01 | 0.72700 | 0.20200 | 4.89e-02 | 0.196000 | 7.89e-01 | 2.84e-01 | 
| Disorders of Nervous System Development | 10 | 4.42e-01 | 0.72700 | 0.20200 | 4.89e-02 | 0.196000 | 7.89e-01 | 2.84e-01 | 
| Loss of function of MECP2 in Rett syndrome | 10 | 4.42e-01 | 0.72700 | 0.20200 | 4.89e-02 | 0.196000 | 7.89e-01 | 2.84e-01 | 
| Pervasive developmental disorders | 10 | 4.42e-01 | 0.72700 | 0.20200 | 4.89e-02 | 0.196000 | 7.89e-01 | 2.84e-01 | 
| FLT3 signaling in disease | 23 | 2.88e-01 | 0.62700 | 0.20200 | -1.82e-01 | -0.088100 | 1.32e-01 | 4.65e-01 | 
| FGFR2 alternative splicing | 22 | 3.95e-01 | 0.71200 | 0.20100 | -1.68e-01 | -0.111000 | 1.74e-01 | 3.66e-01 | 
| Kinesins | 31 | 3.32e-01 | 0.67700 | 0.20100 | -1.44e-01 | -0.140000 | 1.65e-01 | 1.77e-01 | 
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 37 | 1.58e-01 | 0.51200 | 0.20100 | -1.77e-01 | -0.094500 | 6.20e-02 | 3.20e-01 | 
| Golgi-to-ER retrograde transport | 90 | 4.00e-02 | 0.30600 | 0.20100 | -1.51e-01 | -0.133000 | 1.37e-02 | 3.00e-02 | 
| Signaling by GPCR | 187 | 1.46e-03 | 0.07410 | 0.20000 | 1.35e-01 | 0.148000 | 1.50e-03 | 5.27e-04 | 
| VEGFR2 mediated vascular permeability | 21 | 3.95e-01 | 0.71200 | 0.20000 | 1.71e-01 | 0.105000 | 1.76e-01 | 4.05e-01 | 
| KSRP (KHSRP) binds and destabilizes mRNA | 15 | 4.28e-01 | 0.71900 | 0.20000 | -8.20e-02 | -0.183000 | 5.83e-01 | 2.21e-01 | 
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 12 | 5.90e-01 | 0.80200 | 0.20000 | -1.06e-01 | -0.170000 | 5.26e-01 | 3.08e-01 | 
| Interleukin-1 signaling | 72 | 5.91e-02 | 0.37200 | 0.20000 | -1.17e-01 | -0.162000 | 8.68e-02 | 1.74e-02 | 
| Pre-NOTCH Expression and Processing | 41 | 6.96e-03 | 0.13300 | 0.20000 | 2.00e-01 | -0.001610 | 2.68e-02 | 9.86e-01 | 
| Mitotic Prophase | 70 | 8.64e-02 | 0.42200 | 0.20000 | -1.38e-01 | -0.145000 | 4.68e-02 | 3.63e-02 | 
| SUMOylation of SUMOylation proteins | 30 | 3.23e-01 | 0.66700 | 0.20000 | -1.58e-01 | -0.122000 | 1.35e-01 | 2.46e-01 | 
| Diseases associated with N-glycosylation of proteins | 18 | 4.31e-01 | 0.72100 | 0.20000 | -9.90e-02 | -0.173000 | 4.67e-01 | 2.03e-01 | 
| Interactions of Rev with host cellular proteins | 32 | 1.25e-01 | 0.48900 | 0.19900 | -1.87e-01 | -0.068200 | 6.68e-02 | 5.05e-01 | 
| TRAF3-dependent IRF activation pathway | 14 | 3.33e-01 | 0.67700 | 0.19900 | 4.95e-02 | 0.193000 | 7.48e-01 | 2.11e-01 | 
| Interferon Signaling | 130 | 2.46e-03 | 0.08000 | 0.19900 | -1.73e-01 | -0.097500 | 6.84e-04 | 5.59e-02 | 
| MAPK6/MAPK4 signaling | 63 | 1.10e-01 | 0.46300 | 0.19800 | -1.50e-01 | -0.129000 | 3.98e-02 | 7.79e-02 | 
| Synthesis of glycosylphosphatidylinositol (GPI) | 14 | 5.75e-01 | 0.79500 | 0.19700 | -1.12e-01 | -0.162000 | 4.67e-01 | 2.93e-01 | 
| Signaling by FGFR2 IIIa TM | 15 | 5.95e-01 | 0.80300 | 0.19600 | -1.48e-01 | -0.129000 | 3.20e-01 | 3.87e-01 | 
| Signaling by NODAL | 11 | 1.59e-01 | 0.51200 | 0.19600 | -6.56e-02 | 0.185000 | 7.07e-01 | 2.88e-01 | 
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 11 | 5.00e-01 | 0.76000 | 0.19600 | 1.84e-01 | 0.066900 | 2.90e-01 | 7.01e-01 | 
| Post-translational protein phosphorylation | 32 | 3.21e-01 | 0.66500 | 0.19600 | 1.53e-01 | 0.123000 | 1.36e-01 | 2.28e-01 | 
| Signaling by BRAF and RAF1 fusions | 41 | 1.70e-01 | 0.51200 | 0.19600 | 1.68e-01 | 0.101000 | 6.28e-02 | 2.65e-01 | 
| Integration of energy metabolism | 52 | 4.33e-02 | 0.32000 | 0.19600 | 1.83e-01 | 0.070100 | 2.27e-02 | 3.82e-01 | 
| Signaling by SCF-KIT | 31 | 3.53e-01 | 0.69300 | 0.19600 | 1.35e-01 | 0.141000 | 1.93e-01 | 1.73e-01 | 
| FGFR2 mutant receptor activation | 16 | 5.81e-01 | 0.79800 | 0.19500 | -1.46e-01 | -0.129000 | 3.12e-01 | 3.71e-01 | 
| Signaling by FGFR | 50 | 1.26e-01 | 0.48900 | 0.19500 | -1.65e-01 | -0.103000 | 4.32e-02 | 2.09e-01 | 
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 33 | 3.31e-01 | 0.67700 | 0.19400 | 1.30e-01 | 0.144000 | 1.96e-01 | 1.52e-01 | 
| Interferon alpha/beta signaling | 46 | 5.94e-02 | 0.37200 | 0.19400 | -1.82e-01 | -0.066400 | 3.26e-02 | 4.36e-01 | 
| Downregulation of TGF-beta receptor signaling | 25 | 3.30e-01 | 0.67600 | 0.19400 | 9.54e-02 | 0.169000 | 4.10e-01 | 1.44e-01 | 
| Apoptotic factor-mediated response | 14 | 7.01e-02 | 0.39000 | 0.19400 | -1.20e-01 | 0.152000 | 4.37e-01 | 3.25e-01 | 
| XBP1(S) activates chaperone genes | 39 | 2.80e-01 | 0.62300 | 0.19300 | -1.38e-01 | -0.135000 | 1.36e-01 | 1.45e-01 | 
| TNF signaling | 35 | 2.94e-01 | 0.63200 | 0.19300 | -1.19e-01 | -0.152000 | 2.23e-01 | 1.20e-01 | 
| G-protein mediated events | 27 | 2.42e-02 | 0.23100 | 0.19300 | 1.90e-01 | -0.032900 | 8.78e-02 | 7.68e-01 | 
| Signaling by cytosolic FGFR1 fusion mutants | 16 | 1.39e-01 | 0.49100 | 0.19200 | -1.53e-02 | 0.192000 | 9.16e-01 | 1.84e-01 | 
| ABC-family proteins mediated transport | 69 | 9.39e-02 | 0.43600 | 0.19200 | -1.20e-01 | -0.151000 | 8.64e-02 | 3.09e-02 | 
| Drug ADME | 25 | 4.46e-01 | 0.73100 | 0.19200 | 1.36e-01 | 0.136000 | 2.40e-01 | 2.41e-01 | 
| Ribosomal scanning and start codon recognition | 45 | 7.30e-02 | 0.39500 | 0.19200 | -6.81e-02 | -0.179000 | 4.30e-01 | 3.78e-02 | 
| GPCR downstream signalling | 170 | 4.57e-03 | 0.11200 | 0.19100 | 1.38e-01 | 0.133000 | 2.05e-03 | 2.91e-03 | 
| Regulation of IFNA/IFNB signaling | 11 | 1.28e-01 | 0.48900 | 0.19100 | -1.43e-01 | 0.127000 | 4.12e-01 | 4.65e-01 | 
| Transport of inorganic cations/anions and amino acids/oligopeptides | 38 | 1.69e-01 | 0.51200 | 0.19100 | 1.70e-01 | 0.086900 | 6.93e-02 | 3.54e-01 | 
| UCH proteinases | 69 | 1.11e-01 | 0.46300 | 0.19100 | -1.37e-01 | -0.133000 | 4.89e-02 | 5.66e-02 | 
| RUNX2 regulates bone development | 16 | 2.37e-01 | 0.59500 | 0.19100 | 2.43e-02 | 0.189000 | 8.66e-01 | 1.90e-01 | 
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 14 | 5.98e-01 | 0.80300 | 0.19100 | -1.57e-01 | -0.109000 | 3.11e-01 | 4.82e-01 | 
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 14 | 5.98e-01 | 0.80300 | 0.19100 | -1.57e-01 | -0.109000 | 3.11e-01 | 4.82e-01 | 
| Glycogen metabolism | 17 | 4.50e-01 | 0.73200 | 0.19000 | -8.54e-02 | -0.170000 | 5.42e-01 | 2.25e-01 | 
| Metabolism of polyamines | 44 | 1.58e-01 | 0.51200 | 0.19000 | -1.65e-01 | -0.095000 | 5.89e-02 | 2.76e-01 | 
| AURKA Activation by TPX2 | 55 | 1.56e-01 | 0.51200 | 0.19000 | -1.17e-01 | -0.149000 | 1.32e-01 | 5.56e-02 | 
| Regulation of Apoptosis | 42 | 2.50e-01 | 0.59600 | 0.18900 | -1.47e-01 | -0.119000 | 9.94e-02 | 1.82e-01 | 
| tRNA processing | 86 | 6.37e-02 | 0.37900 | 0.18900 | -1.22e-01 | -0.144000 | 5.20e-02 | 2.12e-02 | 
| Nonhomologous End-Joining (NHEJ) | 27 | 3.94e-01 | 0.71200 | 0.18800 | -1.12e-01 | -0.152000 | 3.15e-01 | 1.73e-01 | 
| Autodegradation of Cdh1 by Cdh1:APC/C | 50 | 2.14e-01 | 0.57200 | 0.18800 | -1.34e-01 | -0.131000 | 1.01e-01 | 1.09e-01 | 
| Oncogene Induced Senescence | 27 | 3.57e-01 | 0.70100 | 0.18700 | -9.92e-02 | -0.159000 | 3.72e-01 | 1.54e-01 | 
| Cholesterol biosynthesis | 20 | 5.31e-01 | 0.77400 | 0.18700 | -1.43e-01 | -0.121000 | 2.70e-01 | 3.50e-01 | 
| APC/C:Cdc20 mediated degradation of mitotic proteins | 58 | 1.70e-01 | 0.51200 | 0.18700 | -1.30e-01 | -0.134000 | 8.62e-02 | 7.85e-02 | 
| Regulation of RUNX3 expression and activity | 46 | 2.32e-01 | 0.58900 | 0.18700 | -1.19e-01 | -0.144000 | 1.62e-01 | 9.21e-02 | 
| PI3K/AKT Signaling in Cancer | 51 | 1.42e-01 | 0.49100 | 0.18600 | -9.67e-02 | -0.159000 | 2.33e-01 | 5.05e-02 | 
| Signaling by ALK fusions and activated point mutants | 42 | 9.68e-02 | 0.44100 | 0.18500 | -1.74e-01 | -0.063200 | 5.19e-02 | 4.79e-01 | 
| Signaling by ALK in cancer | 42 | 9.68e-02 | 0.44100 | 0.18500 | -1.74e-01 | -0.063200 | 5.19e-02 | 4.79e-01 | 
| RNA Polymerase II Pre-transcription Events | 61 | 1.62e-01 | 0.51200 | 0.18400 | -1.36e-01 | -0.123000 | 6.57e-02 | 9.67e-02 | 
| Sema4D in semaphorin signaling | 13 | 2.66e-01 | 0.61200 | 0.18400 | -1.84e-01 | 0.000838 | 2.51e-01 | 9.96e-01 | 
| APC/C:Cdc20 mediated degradation of Securin | 51 | 2.18e-01 | 0.57400 | 0.18400 | -1.37e-01 | -0.123000 | 9.18e-02 | 1.30e-01 | 
| Rev-mediated nuclear export of HIV RNA | 31 | 1.41e-01 | 0.49100 | 0.18300 | -1.76e-01 | -0.050200 | 8.94e-02 | 6.29e-01 | 
| CDC42 GTPase cycle | 88 | 5.73e-02 | 0.37200 | 0.18300 | 1.09e-01 | 0.148000 | 7.92e-02 | 1.69e-02 | 
| Regulation of TNFR1 signaling | 30 | 3.32e-01 | 0.67700 | 0.18300 | -9.63e-02 | -0.156000 | 3.62e-01 | 1.41e-01 | 
| Dectin-1 mediated noncanonical NF-kB signaling | 47 | 2.48e-01 | 0.59600 | 0.18300 | -1.36e-01 | -0.122000 | 1.07e-01 | 1.47e-01 | 
| Gene Silencing by RNA | 56 | 1.14e-01 | 0.46300 | 0.18300 | -1.59e-01 | -0.091000 | 4.05e-02 | 2.40e-01 | 
| DNA Damage Recognition in GG-NER | 35 | 3.59e-01 | 0.70200 | 0.18300 | -1.30e-01 | -0.129000 | 1.85e-01 | 1.88e-01 | 
| Cross-presentation of soluble exogenous antigens (endosomes) | 35 | 3.60e-01 | 0.70200 | 0.18300 | -1.30e-01 | -0.128000 | 1.83e-01 | 1.91e-01 | 
| RAC1 GTPase cycle | 99 | 3.85e-02 | 0.29800 | 0.18300 | 1.06e-01 | 0.149000 | 6.97e-02 | 1.07e-02 | 
| Activation of NF-kappaB in B cells | 53 | 1.62e-01 | 0.51200 | 0.18300 | -1.52e-01 | -0.102000 | 5.66e-02 | 2.01e-01 | 
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 57 | 1.88e-01 | 0.53400 | 0.18300 | -1.34e-01 | -0.124000 | 8.02e-02 | 1.06e-01 | 
| SCF-beta-TrCP mediated degradation of Emi1 | 44 | 2.52e-01 | 0.59800 | 0.18200 | -1.44e-01 | -0.111000 | 9.80e-02 | 2.03e-01 | 
| Formation of Incision Complex in GG-NER | 35 | 2.96e-01 | 0.63300 | 0.18200 | 1.52e-01 | 0.100000 | 1.20e-01 | 3.06e-01 | 
| Arachidonic acid metabolism | 19 | 5.16e-01 | 0.77300 | 0.18200 | 9.99e-02 | 0.152000 | 4.51e-01 | 2.51e-01 | 
| Defective Intrinsic Pathway for Apoptosis | 23 | 2.31e-01 | 0.58900 | 0.18200 | 1.76e-01 | 0.047700 | 1.45e-01 | 6.92e-01 | 
| Regulation of PLK1 Activity at G2/M Transition | 67 | 1.33e-01 | 0.49100 | 0.18200 | -1.16e-01 | -0.140000 | 1.02e-01 | 4.73e-02 | 
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 59 | 1.82e-01 | 0.52300 | 0.18100 | -1.24e-01 | -0.132000 | 9.98e-02 | 7.90e-02 | 
| Translation | 228 | 1.03e-03 | 0.06320 | 0.18100 | -1.43e-01 | -0.111000 | 2.22e-04 | 4.14e-03 | 
| Pausing and recovery of Tat-mediated HIV elongation | 22 | 3.86e-01 | 0.71200 | 0.18100 | -7.91e-02 | -0.162000 | 5.21e-01 | 1.88e-01 | 
| Tat-mediated HIV elongation arrest and recovery | 22 | 3.86e-01 | 0.71200 | 0.18100 | -7.91e-02 | -0.162000 | 5.21e-01 | 1.88e-01 | 
| Disorders of transmembrane transporters | 103 | 4.94e-02 | 0.34800 | 0.18000 | -1.16e-01 | -0.138000 | 4.34e-02 | 1.59e-02 | 
| Regulation of signaling by CBL | 13 | 1.87e-01 | 0.53400 | 0.18000 | -1.75e-01 | 0.042900 | 2.76e-01 | 7.89e-01 | 
| RHOQ GTPase cycle | 36 | 3.61e-01 | 0.70400 | 0.18000 | 1.26e-01 | 0.128000 | 1.93e-01 | 1.83e-01 | 
| N-glycan antennae elongation in the medial/trans-Golgi | 18 | 5.62e-01 | 0.78700 | 0.17900 | 1.46e-01 | 0.103000 | 2.83e-01 | 4.48e-01 | 
| Regulated Necrosis | 41 | 2.70e-01 | 0.61600 | 0.17900 | -1.03e-01 | -0.146000 | 2.54e-01 | 1.06e-01 | 
| Triglyceride metabolism | 15 | 5.85e-01 | 0.79900 | 0.17700 | 1.52e-01 | 0.090500 | 3.07e-01 | 5.44e-01 | 
| Signaling by FGFR1 | 27 | 3.43e-01 | 0.68300 | 0.17700 | -1.57e-01 | -0.080800 | 1.58e-01 | 4.68e-01 | 
| Pyruvate metabolism | 18 | 1.63e-01 | 0.51200 | 0.17600 | -1.06e-02 | 0.176000 | 9.38e-01 | 1.97e-01 | 
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 56 | 2.19e-01 | 0.57500 | 0.17500 | -1.30e-01 | -0.118000 | 9.36e-02 | 1.29e-01 | 
| Class I peroxisomal membrane protein import | 17 | 5.54e-01 | 0.78700 | 0.17500 | -8.96e-02 | -0.150000 | 5.23e-01 | 2.83e-01 | 
| M Phase | 273 | 7.25e-04 | 0.05860 | 0.17500 | -1.17e-01 | -0.130000 | 9.30e-04 | 2.48e-04 | 
| Translesion synthesis by POLI | 15 | 4.20e-01 | 0.71800 | 0.17500 | -4.73e-02 | -0.168000 | 7.51e-01 | 2.59e-01 | 
| Metabolism of RNA | 509 | 1.01e-06 | 0.00118 | 0.17500 | -1.08e-01 | -0.137000 | 3.94e-05 | 1.78e-07 | 
| Metabolism of nitric oxide: NOS3 activation and regulation | 12 | 5.67e-01 | 0.79000 | 0.17400 | 1.62e-01 | 0.064000 | 3.30e-01 | 7.01e-01 | 
| Signaling by EGFR in Cancer | 16 | 6.41e-01 | 0.83200 | 0.17400 | -1.09e-01 | -0.135000 | 4.49e-01 | 3.51e-01 | 
| Mitotic Spindle Checkpoint | 91 | 6.85e-02 | 0.38700 | 0.17300 | -1.01e-01 | -0.141000 | 9.67e-02 | 2.06e-02 | 
| Anchoring of the basal body to the plasma membrane | 72 | 1.01e-01 | 0.44900 | 0.17300 | -9.35e-02 | -0.146000 | 1.71e-01 | 3.30e-02 | 
| Vitamin B5 (pantothenate) metabolism | 11 | 4.38e-01 | 0.72700 | 0.17300 | -1.95e-02 | -0.171000 | 9.11e-01 | 3.25e-01 | 
| Synthesis of bile acids and bile salts | 12 | 3.73e-01 | 0.71100 | 0.17200 | 1.72e-01 | 0.009320 | 3.02e-01 | 9.55e-01 | 
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 27 | 4.95e-01 | 0.75800 | 0.17200 | -1.25e-01 | -0.119000 | 2.63e-01 | 2.86e-01 | 
| RAS processing | 13 | 5.97e-01 | 0.80300 | 0.17200 | 7.40e-02 | 0.155000 | 6.44e-01 | 3.34e-01 | 
| Diseases of carbohydrate metabolism | 23 | 2.53e-01 | 0.60000 | 0.17100 | 3.99e-02 | 0.167000 | 7.41e-01 | 1.67e-01 | 
| Regulation of expression of SLITs and ROBOs | 118 | 5.11e-02 | 0.35400 | 0.17000 | -1.25e-01 | -0.115000 | 1.95e-02 | 3.18e-02 | 
| Non-integrin membrane-ECM interactions | 11 | 6.68e-01 | 0.85100 | 0.17000 | 1.51e-01 | 0.077500 | 3.87e-01 | 6.56e-01 | 
| TAK1-dependent IKK and NF-kappa-B activation | 17 | 4.67e-01 | 0.73800 | 0.16900 | -6.13e-02 | -0.158000 | 6.62e-01 | 2.61e-01 | 
| activated TAK1 mediates p38 MAPK activation | 12 | 3.24e-01 | 0.66700 | 0.16900 | 1.19e-02 | -0.168000 | 9.43e-01 | 3.12e-01 | 
| Cell Cycle | 483 | 7.95e-06 | 0.00465 | 0.16800 | -1.10e-01 | -0.127000 | 4.27e-05 | 2.25e-06 | 
| Extracellular matrix organization | 73 | 7.83e-02 | 0.41000 | 0.16800 | 1.49e-01 | 0.079000 | 2.85e-02 | 2.44e-01 | 
| Aquaporin-mediated transport | 19 | 3.93e-01 | 0.71200 | 0.16800 | 5.24e-02 | 0.160000 | 6.92e-01 | 2.29e-01 | 
| IRE1alpha activates chaperones | 40 | 3.74e-01 | 0.71100 | 0.16800 | -1.20e-01 | -0.117000 | 1.90e-01 | 2.00e-01 | 
| Smooth Muscle Contraction | 19 | 6.27e-01 | 0.82400 | 0.16700 | -1.20e-01 | -0.117000 | 3.66e-01 | 3.77e-01 | 
| HIV elongation arrest and recovery | 23 | 4.57e-01 | 0.73600 | 0.16700 | -7.98e-02 | -0.147000 | 5.08e-01 | 2.23e-01 | 
| Pausing and recovery of HIV elongation | 23 | 4.57e-01 | 0.73600 | 0.16700 | -7.98e-02 | -0.147000 | 5.08e-01 | 2.23e-01 | 
| Apoptotic cleavage of cellular proteins | 22 | 1.28e-01 | 0.48900 | 0.16700 | 1.67e-01 | -0.013800 | 1.77e-01 | 9.11e-01 | 
| rRNA modification in the nucleus and cytosol | 44 | 2.32e-02 | 0.22800 | 0.16700 | 3.07e-03 | -0.167000 | 9.72e-01 | 5.56e-02 | 
| GAB1 signalosome | 10 | 4.61e-01 | 0.73800 | 0.16700 | 1.67e-01 | 0.008720 | 3.62e-01 | 9.62e-01 | 
| Mitochondrial translation | 84 | 7.45e-03 | 0.13600 | 0.16700 | -1.63e-01 | -0.035700 | 1.00e-02 | 5.72e-01 | 
| Peptide hormone metabolism | 27 | 5.14e-01 | 0.77200 | 0.16600 | 1.25e-01 | 0.110000 | 2.63e-01 | 3.23e-01 | 
| Degradation of the extracellular matrix | 28 | 4.70e-01 | 0.73800 | 0.16600 | 1.34e-01 | 0.098000 | 2.19e-01 | 3.70e-01 | 
| RUNX3 regulates NOTCH signaling | 11 | 3.74e-01 | 0.71100 | 0.16600 | 1.66e-01 | -0.009500 | 3.41e-01 | 9.57e-01 | 
| RHOG GTPase cycle | 44 | 5.14e-02 | 0.35400 | 0.16600 | 2.15e-02 | 0.165000 | 8.05e-01 | 5.92e-02 | 
| RHOJ GTPase cycle | 34 | 4.31e-01 | 0.72100 | 0.16600 | 1.26e-01 | 0.108000 | 2.04e-01 | 2.76e-01 | 
| Orc1 removal from chromatin | 53 | 2.81e-01 | 0.62300 | 0.16500 | -1.15e-01 | -0.119000 | 1.49e-01 | 1.34e-01 | 
| Regulation of TP53 Activity | 128 | 2.56e-02 | 0.23500 | 0.16500 | -9.03e-02 | -0.139000 | 7.87e-02 | 6.96e-03 | 
| Suppression of phagosomal maturation | 11 | 7.27e-01 | 0.89000 | 0.16500 | -1.39e-01 | -0.089900 | 4.26e-01 | 6.06e-01 | 
| G2/M Transition | 145 | 3.10e-02 | 0.26300 | 0.16500 | -1.23e-01 | -0.110000 | 1.07e-02 | 2.30e-02 | 
| Formation of tubulin folding intermediates by CCT/TriC | 13 | 5.07e-01 | 0.76700 | 0.16500 | -1.59e-01 | -0.043200 | 3.21e-01 | 7.87e-01 | 
| tRNA modification in the nucleus and cytosol | 30 | 2.88e-01 | 0.62700 | 0.16400 | -6.11e-02 | -0.153000 | 5.63e-01 | 1.48e-01 | 
| Cell-Cell communication | 41 | 2.22e-01 | 0.58000 | 0.16400 | 6.95e-02 | 0.148000 | 4.42e-01 | 1.00e-01 | 
| Regulation of PTEN stability and activity | 52 | 2.10e-01 | 0.56600 | 0.16300 | -8.39e-02 | -0.140000 | 2.96e-01 | 8.06e-02 | 
| Unwinding of DNA | 10 | 4.75e-01 | 0.73800 | 0.16300 | 1.63e-01 | 0.007950 | 3.72e-01 | 9.65e-01 | 
| RND3 GTPase cycle | 29 | 3.18e-01 | 0.66200 | 0.16300 | 6.26e-02 | 0.150000 | 5.60e-01 | 1.61e-01 | 
| The citric acid (TCA) cycle and respiratory electron transport | 109 | 5.88e-02 | 0.37200 | 0.16300 | -1.32e-01 | -0.094600 | 1.73e-02 | 8.90e-02 | 
| HCMV Infection | 67 | 2.12e-01 | 0.56800 | 0.16200 | -1.19e-01 | -0.111000 | 9.32e-02 | 1.18e-01 | 
| Regulation of RUNX2 expression and activity | 54 | 2.88e-01 | 0.62700 | 0.16200 | -1.12e-01 | -0.118000 | 1.57e-01 | 1.35e-01 | 
| Regulation of BACH1 activity | 11 | 2.56e-01 | 0.60300 | 0.16200 | -1.45e-01 | 0.073300 | 4.07e-01 | 6.74e-01 | 
| Deactivation of the beta-catenin transactivating complex | 26 | 4.06e-01 | 0.71500 | 0.16200 | -1.45e-01 | -0.070900 | 2.00e-01 | 5.32e-01 | 
| Downstream TCR signaling | 64 | 1.69e-01 | 0.51200 | 0.16200 | -1.36e-01 | -0.087200 | 6.03e-02 | 2.28e-01 | 
| Glucagon signaling in metabolic regulation | 14 | 7.12e-01 | 0.88000 | 0.16100 | 9.94e-02 | 0.126000 | 5.20e-01 | 4.13e-01 | 
| SUMOylation of DNA methylation proteins | 14 | 7.29e-01 | 0.89100 | 0.16100 | 1.14e-01 | 0.113000 | 4.61e-01 | 4.63e-01 | 
| Cellular response to hypoxia | 56 | 2.36e-01 | 0.59500 | 0.16000 | -1.31e-01 | -0.090500 | 8.95e-02 | 2.42e-01 | 
| Protein-protein interactions at synapses | 31 | 4.99e-01 | 0.76000 | 0.15900 | 1.07e-01 | 0.118000 | 3.04e-01 | 2.56e-01 | 
| Hedgehog ‘off’ state | 70 | 1.74e-01 | 0.51400 | 0.15900 | -1.29e-01 | -0.091900 | 6.16e-02 | 1.84e-01 | 
| Membrane binding and targetting of GAG proteins | 11 | 3.42e-01 | 0.68300 | 0.15800 | 1.55e-01 | -0.034000 | 3.75e-01 | 8.45e-01 | 
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 11 | 3.42e-01 | 0.68300 | 0.15800 | 1.55e-01 | -0.034000 | 3.75e-01 | 8.45e-01 | 
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 57 | 2.85e-01 | 0.62600 | 0.15800 | -1.08e-01 | -0.116000 | 1.61e-01 | 1.30e-01 | 
| p75 NTR receptor-mediated signalling | 53 | 1.40e-01 | 0.49100 | 0.15800 | -1.46e-01 | -0.060800 | 6.65e-02 | 4.45e-01 | 
| Mitochondrial translation termination | 78 | 8.59e-03 | 0.14500 | 0.15800 | -1.57e-01 | -0.020400 | 1.69e-02 | 7.56e-01 | 
| Metabolism of cofactors | 16 | 6.73e-01 | 0.85100 | 0.15800 | 1.29e-01 | 0.091900 | 3.74e-01 | 5.25e-01 | 
| Regulation of PTEN gene transcription | 44 | 2.46e-01 | 0.59600 | 0.15800 | -1.41e-01 | -0.071600 | 1.07e-01 | 4.11e-01 | 
| HDACs deacetylate histones | 28 | 2.38e-01 | 0.59500 | 0.15800 | -1.54e-01 | -0.035800 | 1.60e-01 | 7.43e-01 | 
| TP53 Regulates Transcription of Cell Death Genes | 29 | 4.00e-01 | 0.71200 | 0.15800 | 7.21e-02 | 0.140000 | 5.02e-01 | 1.91e-01 | 
| SLC-mediated transmembrane transport | 91 | 1.13e-01 | 0.46300 | 0.15800 | 1.27e-01 | 0.093600 | 3.70e-02 | 1.24e-01 | 
| Mitotic Metaphase and Anaphase | 181 | 2.09e-02 | 0.22800 | 0.15700 | -1.13e-01 | -0.110000 | 9.30e-03 | 1.11e-02 | 
| Regulation of insulin secretion | 33 | 1.12e-01 | 0.46300 | 0.15700 | 1.57e-01 | 0.011500 | 1.19e-01 | 9.09e-01 | 
| Collagen biosynthesis and modifying enzymes | 13 | 7.39e-01 | 0.89100 | 0.15700 | 1.24e-01 | 0.096800 | 4.40e-01 | 5.46e-01 | 
| Abortive elongation of HIV-1 transcript in the absence of Tat | 18 | 6.59e-01 | 0.84700 | 0.15700 | -1.24e-01 | -0.097200 | 3.64e-01 | 4.75e-01 | 
| Interleukin-7 signaling | 14 | 2.12e-01 | 0.56800 | 0.15700 | -5.91e-02 | 0.146000 | 7.02e-01 | 3.46e-01 | 
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | 82 | 8.20e-02 | 0.41800 | 0.15700 | -1.39e-01 | -0.073600 | 3.01e-02 | 2.50e-01 | 
| Transport to the Golgi and subsequent modification | 122 | 6.40e-02 | 0.37900 | 0.15700 | -9.84e-02 | -0.122000 | 6.14e-02 | 2.02e-02 | 
| Cleavage of the damaged purine | 10 | 3.79e-01 | 0.71100 | 0.15700 | -1.52e-01 | 0.036300 | 4.04e-01 | 8.42e-01 | 
| Depurination | 10 | 3.79e-01 | 0.71100 | 0.15700 | -1.52e-01 | 0.036300 | 4.04e-01 | 8.42e-01 | 
| Recognition and association of DNA glycosylase with site containing an affected purine | 10 | 3.79e-01 | 0.71100 | 0.15700 | -1.52e-01 | 0.036300 | 4.04e-01 | 8.42e-01 | 
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 12 | 7.50e-01 | 0.89700 | 0.15600 | -1.27e-01 | -0.092100 | 4.48e-01 | 5.81e-01 | 
| Signaling by NOTCH4 | 65 | 2.46e-01 | 0.59600 | 0.15600 | -1.16e-01 | -0.105000 | 1.06e-01 | 1.45e-01 | 
| Response of Mtb to phagocytosis | 19 | 6.64e-01 | 0.84800 | 0.15500 | -1.16e-01 | -0.103000 | 3.80e-01 | 4.37e-01 | 
| Intra-Golgi and retrograde Golgi-to-ER traffic | 150 | 2.34e-02 | 0.22800 | 0.15500 | -8.53e-02 | -0.130000 | 7.26e-02 | 6.26e-03 | 
| Glucose metabolism | 68 | 1.45e-01 | 0.49400 | 0.15500 | -1.35e-01 | -0.076400 | 5.42e-02 | 2.77e-01 | 
| Mitotic G2-G2/M phases | 147 | 4.68e-02 | 0.33800 | 0.15500 | -1.11e-01 | -0.108000 | 2.04e-02 | 2.44e-02 | 
| FCERI mediated MAPK activation | 21 | 7.64e-02 | 0.40600 | 0.15500 | -1.12e-01 | 0.107000 | 3.76e-01 | 3.96e-01 | 
| Energy dependent regulation of mTOR by LKB1-AMPK | 21 | 4.05e-01 | 0.71500 | 0.15400 | 1.47e-01 | 0.045000 | 2.42e-01 | 7.21e-01 | 
| Activation of BH3-only proteins | 25 | 5.94e-01 | 0.80300 | 0.15400 | 1.12e-01 | 0.106000 | 3.33e-01 | 3.61e-01 | 
| Mitochondrial translation initiation | 79 | 7.38e-03 | 0.13600 | 0.15400 | -1.53e-01 | -0.012700 | 1.89e-02 | 8.46e-01 | 
| Interleukin-1 family signaling | 89 | 1.06e-01 | 0.45700 | 0.15300 | -8.20e-02 | -0.130000 | 1.82e-01 | 3.51e-02 | 
| Mitotic Anaphase | 180 | 2.60e-02 | 0.23500 | 0.15300 | -1.09e-01 | -0.107000 | 1.18e-02 | 1.34e-02 | 
| Toll Like Receptor 9 (TLR9) Cascade | 64 | 1.64e-01 | 0.51200 | 0.15300 | -1.34e-01 | -0.073500 | 6.35e-02 | 3.10e-01 | 
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 61 | 2.29e-01 | 0.58800 | 0.15300 | -1.27e-01 | -0.085200 | 8.63e-02 | 2.51e-01 | 
| Biological oxidations | 73 | 1.39e-01 | 0.49100 | 0.15300 | 7.66e-02 | 0.132000 | 2.59e-01 | 5.07e-02 | 
| Transport of bile salts and organic acids, metal ions and amine compounds | 31 | 5.11e-01 | 0.76900 | 0.15300 | 9.54e-02 | 0.119000 | 3.58e-01 | 2.50e-01 | 
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 37 | 1.31e-01 | 0.49100 | 0.15300 | -2.33e-02 | -0.151000 | 8.06e-01 | 1.13e-01 | 
| mRNA Splicing - Minor Pathway | 43 | 4.04e-01 | 0.71500 | 0.15200 | -9.75e-02 | -0.117000 | 2.69e-01 | 1.85e-01 | 
| FCERI mediated NF-kB activation | 59 | 2.84e-01 | 0.62600 | 0.15200 | -1.19e-01 | -0.094900 | 1.16e-01 | 2.08e-01 | 
| Basigin interactions | 13 | 5.64e-01 | 0.78800 | 0.15100 | 3.99e-02 | 0.146000 | 8.04e-01 | 3.62e-01 | 
| Signaling by NTRK3 (TRKC) | 10 | 6.65e-01 | 0.84800 | 0.15100 | 4.56e-02 | 0.144000 | 8.03e-01 | 4.29e-01 | 
| Intraflagellar transport | 30 | 3.21e-01 | 0.66500 | 0.15100 | -5.09e-02 | -0.143000 | 6.30e-01 | 1.77e-01 | 
| Circadian Clock | 51 | 2.48e-01 | 0.59600 | 0.15100 | 1.32e-01 | 0.073500 | 1.03e-01 | 3.64e-01 | 
| MyD88 dependent cascade initiated on endosome | 62 | 1.81e-01 | 0.52300 | 0.15100 | -1.33e-01 | -0.071900 | 7.16e-02 | 3.28e-01 | 
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 62 | 1.81e-01 | 0.52300 | 0.15100 | -1.33e-01 | -0.071900 | 7.16e-02 | 3.28e-01 | 
| Metabolism of steroid hormones | 13 | 7.32e-01 | 0.89100 | 0.15100 | -1.26e-01 | -0.082400 | 4.31e-01 | 6.07e-01 | 
| Ion channel transport | 76 | 1.36e-01 | 0.49100 | 0.15000 | 1.30e-01 | 0.074500 | 4.97e-02 | 2.62e-01 | 
| SUMOylation of transcription cofactors | 35 | 2.73e-01 | 0.61700 | 0.15000 | 5.04e-02 | 0.141000 | 6.06e-01 | 1.49e-01 | 
| TRAF6 mediated NF-kB activation | 19 | 4.51e-01 | 0.73200 | 0.15000 | -1.44e-01 | -0.041400 | 2.78e-01 | 7.55e-01 | 
| APC/C-mediated degradation of cell cycle proteins | 70 | 2.50e-01 | 0.59600 | 0.14900 | -9.93e-02 | -0.112000 | 1.52e-01 | 1.07e-01 | 
| Regulation of mitotic cell cycle | 70 | 2.50e-01 | 0.59600 | 0.14900 | -9.93e-02 | -0.112000 | 1.52e-01 | 1.07e-01 | 
| SRP-dependent cotranslational protein targeting to membrane | 86 | 1.84e-01 | 0.52800 | 0.14800 | -1.13e-01 | -0.095600 | 7.09e-02 | 1.26e-01 | 
| Cell Cycle, Mitotic | 390 | 7.52e-04 | 0.05860 | 0.14800 | -1.02e-01 | -0.107000 | 6.06e-04 | 3.55e-04 | 
| COPI-independent Golgi-to-ER retrograde traffic | 28 | 5.58e-01 | 0.78700 | 0.14700 | -8.86e-02 | -0.118000 | 4.17e-01 | 2.81e-01 | 
| Josephin domain DUBs | 11 | 7.52e-01 | 0.89700 | 0.14700 | -1.29e-01 | -0.071100 | 4.60e-01 | 6.83e-01 | 
| Death Receptor Signalling | 86 | 1.60e-01 | 0.51200 | 0.14700 | -1.20e-01 | -0.085000 | 5.55e-02 | 1.74e-01 | 
| Signaling by RAF1 mutants | 25 | 5.86e-01 | 0.79900 | 0.14600 | 1.20e-01 | 0.084000 | 3.01e-01 | 4.68e-01 | 
| CDK-mediated phosphorylation and removal of Cdc6 | 56 | 3.51e-01 | 0.69300 | 0.14600 | -1.07e-01 | -0.099300 | 1.68e-01 | 1.99e-01 | 
| Interconversion of nucleotide di- and triphosphates | 18 | 2.83e-01 | 0.62500 | 0.14600 | -1.06e-02 | 0.145000 | 9.38e-01 | 2.86e-01 | 
| Estrogen-dependent gene expression | 67 | 9.70e-02 | 0.44100 | 0.14500 | -1.37e-01 | -0.048700 | 5.31e-02 | 4.91e-01 | 
| HCMV Late Events | 47 | 3.97e-01 | 0.71200 | 0.14500 | -8.98e-02 | -0.114000 | 2.87e-01 | 1.77e-01 | 
| Interleukin-4 and Interleukin-13 signaling | 48 | 7.16e-02 | 0.39200 | 0.14500 | -1.44e-01 | -0.012900 | 8.39e-02 | 8.77e-01 | 
| Fatty acyl-CoA biosynthesis | 19 | 1.39e-01 | 0.49100 | 0.14500 | -8.06e-02 | 0.120000 | 5.43e-01 | 3.64e-01 | 
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 18 | 5.77e-01 | 0.79500 | 0.14500 | -1.33e-01 | -0.057100 | 3.29e-01 | 6.75e-01 | 
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 26 | 6.17e-01 | 0.82300 | 0.14500 | -9.71e-02 | -0.107000 | 3.92e-01 | 3.44e-01 | 
| Azathioprine ADME | 15 | 7.51e-01 | 0.89700 | 0.14500 | 9.23e-02 | 0.111000 | 5.36e-01 | 4.55e-01 | 
| Transcriptional regulation by RUNX3 | 70 | 2.16e-01 | 0.57300 | 0.14500 | -7.92e-02 | -0.121000 | 2.53e-01 | 8.06e-02 | 
| Loss of Nlp from mitotic centrosomes | 52 | 3.42e-01 | 0.68300 | 0.14400 | -8.34e-02 | -0.118000 | 2.99e-01 | 1.43e-01 | 
| Loss of proteins required for interphase microtubule organization from the centrosome | 52 | 3.42e-01 | 0.68300 | 0.14400 | -8.34e-02 | -0.118000 | 2.99e-01 | 1.43e-01 | 
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 23 | 4.33e-01 | 0.72200 | 0.14400 | -1.37e-01 | -0.043800 | 2.56e-01 | 7.16e-01 | 
| Intra-Golgi traffic | 37 | 3.44e-01 | 0.68300 | 0.14300 | -5.90e-02 | -0.131000 | 5.35e-01 | 1.69e-01 | 
| Initiation of Nuclear Envelope (NE) Reformation | 17 | 4.52e-01 | 0.73200 | 0.14300 | -1.41e-01 | -0.024300 | 3.15e-01 | 8.62e-01 | 
| Signaling by ALK | 17 | 1.97e-01 | 0.54300 | 0.14300 | -1.28e-01 | 0.063400 | 3.61e-01 | 6.51e-01 | 
| RHO GTPase Effectors | 182 | 1.48e-02 | 0.19900 | 0.14300 | -7.17e-02 | -0.123000 | 9.71e-02 | 4.27e-03 | 
| Asparagine N-linked glycosylation | 214 | 2.16e-02 | 0.22800 | 0.14300 | -9.33e-02 | -0.108000 | 1.94e-02 | 6.85e-03 | 
| SARS-CoV-2 Infection | 203 | 2.86e-02 | 0.24600 | 0.14300 | -1.03e-01 | -0.098900 | 1.22e-02 | 1.57e-02 | 
| Centrosome maturation | 60 | 2.85e-01 | 0.62600 | 0.14300 | -7.95e-02 | -0.118000 | 2.88e-01 | 1.14e-01 | 
| Recruitment of mitotic centrosome proteins and complexes | 60 | 2.85e-01 | 0.62600 | 0.14300 | -7.95e-02 | -0.118000 | 2.88e-01 | 1.14e-01 | 
| Early Phase of HIV Life Cycle | 12 | 7.97e-01 | 0.91600 | 0.14200 | -1.12e-01 | -0.088300 | 5.03e-01 | 5.97e-01 | 
| RMTs methylate histone arginines | 24 | 1.28e-01 | 0.48900 | 0.14200 | -4.37e-02 | 0.135000 | 7.11e-01 | 2.51e-01 | 
| Interleukin-15 signaling | 11 | 8.21e-01 | 0.92100 | 0.14200 | 1.05e-01 | 0.095800 | 5.46e-01 | 5.82e-01 | 
| PPARA activates gene expression | 79 | 1.59e-01 | 0.51200 | 0.14200 | 1.23e-01 | 0.070700 | 5.92e-02 | 2.78e-01 | 
| Recruitment of NuMA to mitotic centrosomes | 59 | 2.60e-01 | 0.60300 | 0.14200 | -7.17e-02 | -0.122000 | 3.42e-01 | 1.05e-01 | 
| Metabolism of water-soluble vitamins and cofactors | 76 | 2.57e-01 | 0.60300 | 0.14100 | -9.28e-02 | -0.107000 | 1.63e-01 | 1.08e-01 | 
| Nucleotide salvage | 17 | 6.54e-01 | 0.84300 | 0.14100 | -1.25e-01 | -0.065700 | 3.72e-01 | 6.39e-01 | 
| Pre-NOTCH Transcription and Translation | 27 | 6.52e-02 | 0.37900 | 0.14100 | 9.18e-02 | -0.107000 | 4.10e-01 | 3.36e-01 | 
| DNA strand elongation | 27 | 3.10e-01 | 0.65400 | 0.14100 | -2.74e-02 | -0.138000 | 8.06e-01 | 2.14e-01 | 
| Mitochondrial translation elongation | 79 | 1.05e-02 | 0.16100 | 0.14000 | -1.40e-01 | -0.001400 | 3.17e-02 | 9.83e-01 | 
| Frs2-mediated activation | 11 | 6.55e-01 | 0.84500 | 0.13900 | -1.35e-01 | -0.034700 | 4.38e-01 | 8.42e-01 | 
| Nuclear Envelope Breakdown | 45 | 4.53e-01 | 0.73200 | 0.13900 | -1.07e-01 | -0.089600 | 2.16e-01 | 2.99e-01 | 
| Signaling by FGFR1 in disease | 23 | 1.14e-01 | 0.46300 | 0.13900 | -7.34e-02 | 0.118000 | 5.43e-01 | 3.28e-01 | 
| Degradation of AXIN | 44 | 4.76e-01 | 0.73800 | 0.13800 | -9.34e-02 | -0.102000 | 2.84e-01 | 2.42e-01 | 
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 15 | 4.17e-01 | 0.71800 | 0.13800 | -1.38e-01 | 0.001860 | 3.55e-01 | 9.90e-01 | 
| DNA Damage/Telomere Stress Induced Senescence | 24 | 6.40e-01 | 0.83200 | 0.13800 | -8.14e-02 | -0.111000 | 4.90e-01 | 3.45e-01 | 
| L1CAM interactions | 34 | 5.34e-01 | 0.77400 | 0.13800 | 1.11e-01 | 0.081500 | 2.63e-01 | 4.11e-01 | 
| Formation of RNA Pol II elongation complex | 45 | 4.42e-01 | 0.72700 | 0.13700 | -1.10e-01 | -0.082300 | 2.02e-01 | 3.40e-01 | 
| RNA Polymerase II Transcription Elongation | 45 | 4.42e-01 | 0.72700 | 0.13700 | -1.10e-01 | -0.082300 | 2.02e-01 | 3.40e-01 | 
| PI3K Cascade | 17 | 6.61e-01 | 0.84800 | 0.13700 | -1.22e-01 | -0.061000 | 3.83e-01 | 6.63e-01 | 
| ADORA2B mediated anti-inflammatory cytokines production | 28 | 6.32e-01 | 0.82900 | 0.13700 | 9.36e-02 | 0.099400 | 3.92e-01 | 3.63e-01 | 
| RNA Polymerase I Transcription Termination | 24 | 5.72e-01 | 0.79300 | 0.13600 | 1.21e-01 | 0.062600 | 3.07e-01 | 5.96e-01 | 
| Vasopressin regulates renal water homeostasis via Aquaporins | 18 | 6.36e-01 | 0.83000 | 0.13600 | 5.80e-02 | 0.123000 | 6.70e-01 | 3.67e-01 | 
| MyD88 cascade initiated on plasma membrane | 61 | 2.61e-01 | 0.60300 | 0.13600 | -1.19e-01 | -0.065900 | 1.09e-01 | 3.74e-01 | 
| Toll Like Receptor 10 (TLR10) Cascade | 61 | 2.61e-01 | 0.60300 | 0.13600 | -1.19e-01 | -0.065900 | 1.09e-01 | 3.74e-01 | 
| Toll Like Receptor 5 (TLR5) Cascade | 61 | 2.61e-01 | 0.60300 | 0.13600 | -1.19e-01 | -0.065900 | 1.09e-01 | 3.74e-01 | 
| Negative regulation of MET activity | 14 | 6.97e-01 | 0.86700 | 0.13600 | -5.60e-02 | -0.123000 | 7.17e-01 | 4.24e-01 | 
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 28 | 6.33e-01 | 0.82900 | 0.13600 | -9.02e-02 | -0.101000 | 4.09e-01 | 3.55e-01 | 
| Signaling by ROBO receptors | 146 | 9.22e-02 | 0.43300 | 0.13500 | -8.57e-02 | -0.104000 | 7.49e-02 | 3.13e-02 | 
| Signaling by EGFR | 35 | 1.78e-01 | 0.51900 | 0.13400 | -8.49e-03 | -0.134000 | 9.31e-01 | 1.70e-01 | 
| Assembly Of The HIV Virion | 13 | 4.77e-01 | 0.73900 | 0.13400 | 1.34e-01 | -0.005320 | 4.03e-01 | 9.73e-01 | 
| Signaling by ERBB4 | 29 | 7.49e-02 | 0.40200 | 0.13400 | -1.10e-01 | 0.076100 | 3.04e-01 | 4.78e-01 | 
| SUMOylation of DNA damage response and repair proteins | 64 | 3.59e-01 | 0.70200 | 0.13300 | -1.02e-01 | -0.086600 | 1.61e-01 | 2.31e-01 | 
| Rab regulation of trafficking | 81 | 1.89e-01 | 0.53600 | 0.13300 | -6.66e-02 | -0.116000 | 3.01e-01 | 7.27e-02 | 
| Pyroptosis | 17 | 6.65e-01 | 0.84800 | 0.13300 | 5.71e-02 | 0.120000 | 6.84e-01 | 3.91e-01 | 
| Cyclin E associated events during G1/S transition | 68 | 2.42e-01 | 0.59600 | 0.13300 | -1.16e-01 | -0.065400 | 9.90e-02 | 3.52e-01 | 
| Anti-inflammatory response favouring Leishmania parasite infection | 47 | 4.72e-01 | 0.73800 | 0.13300 | 1.02e-01 | 0.085600 | 2.28e-01 | 3.10e-01 | 
| Leishmania parasite growth and survival | 47 | 4.72e-01 | 0.73800 | 0.13300 | 1.02e-01 | 0.085600 | 2.28e-01 | 3.10e-01 | 
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 15 | 4.51e-01 | 0.73200 | 0.13300 | 1.33e-01 | -0.000373 | 3.73e-01 | 9.98e-01 | 
| Assembly of the pre-replicative complex | 64 | 3.67e-01 | 0.70900 | 0.13300 | -8.83e-02 | -0.099300 | 2.23e-01 | 1.70e-01 | 
| Maturation of nucleoprotein | 11 | 7.92e-01 | 0.91600 | 0.13200 | 6.39e-02 | 0.116000 | 7.14e-01 | 5.05e-01 | 
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 10 | 4.19e-01 | 0.71800 | 0.13200 | 7.46e-02 | -0.109000 | 6.83e-01 | 5.50e-01 | 
| Cyclin A/B1/B2 associated events during G2/M transition | 22 | 7.00e-01 | 0.86900 | 0.13200 | -1.03e-01 | -0.082400 | 4.02e-01 | 5.04e-01 | 
| Signaling by FLT3 ITD and TKD mutants | 12 | 5.99e-01 | 0.80300 | 0.13200 | 1.72e-02 | 0.131000 | 9.18e-01 | 4.32e-01 | 
| Inositol phosphate metabolism | 29 | 2.16e-01 | 0.57300 | 0.13100 | 1.31e-01 | -0.002050 | 2.21e-01 | 9.85e-01 | 
| SARS-CoV Infections | 257 | 1.77e-02 | 0.21400 | 0.13100 | -1.03e-01 | -0.081100 | 4.77e-03 | 2.62e-02 | 
| RAB geranylgeranylation | 37 | 5.08e-01 | 0.76700 | 0.13100 | -7.07e-02 | -0.110000 | 4.57e-01 | 2.47e-01 | 
| Signal amplification | 16 | 4.24e-01 | 0.71800 | 0.13100 | 1.30e-01 | -0.004540 | 3.66e-01 | 9.75e-01 | 
| TP53 Regulates Transcription of DNA Repair Genes | 45 | 4.49e-01 | 0.73200 | 0.13100 | -7.19e-02 | -0.109000 | 4.05e-01 | 2.07e-01 | 
| Regulation of RAS by GAPs | 52 | 4.60e-01 | 0.73800 | 0.13000 | -9.49e-02 | -0.089400 | 2.37e-01 | 2.65e-01 | 
| Regulation of lipid metabolism by PPARalpha | 81 | 1.91e-01 | 0.53900 | 0.13000 | 1.14e-01 | 0.062600 | 7.60e-02 | 3.31e-01 | 
| Interleukin-2 family signaling | 27 | 3.14e-01 | 0.65700 | 0.13000 | 1.40e-02 | 0.129000 | 9.00e-01 | 2.46e-01 | 
| Peroxisomal protein import | 44 | 4.66e-01 | 0.73800 | 0.13000 | -1.08e-01 | -0.072300 | 2.17e-01 | 4.07e-01 | 
| Sulfur amino acid metabolism | 17 | 5.23e-01 | 0.77400 | 0.12900 | -1.28e-01 | -0.022400 | 3.63e-01 | 8.73e-01 | 
| Peroxisomal lipid metabolism | 18 | 5.70e-01 | 0.79100 | 0.12900 | -3.60e-02 | -0.124000 | 7.92e-01 | 3.61e-01 | 
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 13 | 8.21e-01 | 0.92100 | 0.12900 | 9.86e-02 | 0.083900 | 5.39e-01 | 6.01e-01 | 
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 29 | 5.36e-01 | 0.77400 | 0.12900 | 1.15e-01 | 0.058400 | 2.83e-01 | 5.87e-01 | 
| Signaling by RAS mutants | 29 | 5.36e-01 | 0.77400 | 0.12900 | 1.15e-01 | 0.058400 | 2.83e-01 | 5.87e-01 | 
| Signaling by moderate kinase activity BRAF mutants | 29 | 5.36e-01 | 0.77400 | 0.12900 | 1.15e-01 | 0.058400 | 2.83e-01 | 5.87e-01 | 
| Signaling downstream of RAS mutants | 29 | 5.36e-01 | 0.77400 | 0.12900 | 1.15e-01 | 0.058400 | 2.83e-01 | 5.87e-01 | 
| Interleukin receptor SHC signaling | 15 | 3.36e-01 | 0.67800 | 0.12900 | -4.39e-02 | 0.122000 | 7.68e-01 | 4.15e-01 | 
| Cyclin A:Cdk2-associated events at S phase entry | 70 | 2.73e-01 | 0.61700 | 0.12900 | -1.10e-01 | -0.066200 | 1.11e-01 | 3.39e-01 | 
| IGF1R signaling cascade | 21 | 5.61e-01 | 0.78700 | 0.12900 | -1.21e-01 | -0.042900 | 3.36e-01 | 7.34e-01 | 
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 21 | 5.61e-01 | 0.78700 | 0.12900 | -1.21e-01 | -0.042900 | 3.36e-01 | 7.34e-01 | 
| Activation of HOX genes during differentiation | 37 | 5.57e-01 | 0.78700 | 0.12800 | -1.03e-01 | -0.077300 | 2.80e-01 | 4.17e-01 | 
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 37 | 5.57e-01 | 0.78700 | 0.12800 | -1.03e-01 | -0.077300 | 2.80e-01 | 4.17e-01 | 
| Growth hormone receptor signaling | 16 | 2.69e-01 | 0.61600 | 0.12800 | -1.05e-01 | 0.073500 | 4.67e-01 | 6.11e-01 | 
| Notch-HLH transcription pathway | 21 | 4.72e-01 | 0.73800 | 0.12800 | 1.26e-01 | 0.025300 | 3.19e-01 | 8.41e-01 | 
| RNA Polymerase III Transcription Initiation | 35 | 5.97e-01 | 0.80300 | 0.12800 | -8.34e-02 | -0.097000 | 3.93e-01 | 3.21e-01 | 
| TGF-beta receptor signaling activates SMADs | 36 | 5.60e-01 | 0.78700 | 0.12800 | 7.47e-02 | 0.104000 | 4.39e-01 | 2.81e-01 | 
| Influenza Infection | 126 | 1.68e-01 | 0.51200 | 0.12800 | -9.09e-02 | -0.089800 | 7.91e-02 | 8.28e-02 | 
| Gluconeogenesis | 23 | 6.96e-01 | 0.86700 | 0.12700 | -1.03e-01 | -0.075700 | 3.95e-01 | 5.30e-01 | 
| SUMOylation of DNA replication proteins | 41 | 5.52e-01 | 0.78700 | 0.12700 | -9.58e-02 | -0.083900 | 2.89e-01 | 3.53e-01 | 
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 15 | 7.95e-01 | 0.91600 | 0.12700 | 1.01e-01 | 0.077800 | 5.00e-01 | 6.02e-01 | 
| Effects of PIP2 hydrolysis | 18 | 3.86e-01 | 0.71200 | 0.12700 | 1.27e-01 | -0.008410 | 3.52e-01 | 9.51e-01 | 
| FGFR1 mutant receptor activation | 19 | 2.16e-01 | 0.57300 | 0.12700 | -7.42e-02 | 0.103000 | 5.76e-01 | 4.38e-01 | 
| G alpha (s) signalling events | 38 | 4.68e-01 | 0.73800 | 0.12600 | 5.84e-02 | 0.112000 | 5.34e-01 | 2.33e-01 | 
| CLEC7A (Dectin-1) signaling | 77 | 3.37e-01 | 0.67800 | 0.12600 | -8.31e-02 | -0.094700 | 2.08e-01 | 1.52e-01 | 
| Insulin receptor recycling | 17 | 5.94e-01 | 0.80300 | 0.12600 | 1.22e-01 | 0.032700 | 3.85e-01 | 8.16e-01 | 
| Influenza Viral RNA Transcription and Replication | 109 | 2.24e-01 | 0.58100 | 0.12600 | -9.00e-02 | -0.087800 | 1.06e-01 | 1.14e-01 | 
| DNA Repair | 234 | 8.11e-03 | 0.14400 | 0.12600 | -5.48e-02 | -0.113000 | 1.51e-01 | 3.08e-03 | 
| Nuclear events stimulated by ALK signaling in cancer | 13 | 4.28e-01 | 0.71900 | 0.12500 | -1.20e-01 | 0.035400 | 4.53e-01 | 8.25e-01 | 
| MyD88-independent TLR4 cascade | 71 | 3.76e-01 | 0.71100 | 0.12500 | -9.15e-02 | -0.085700 | 1.84e-01 | 2.13e-01 | 
| TRIF(TICAM1)-mediated TLR4 signaling | 71 | 3.76e-01 | 0.71100 | 0.12500 | -9.15e-02 | -0.085700 | 1.84e-01 | 2.13e-01 | 
| Amino acids regulate mTORC1 | 35 | 5.73e-01 | 0.79400 | 0.12500 | -1.03e-01 | -0.070900 | 2.92e-01 | 4.68e-01 | 
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 11 | 4.70e-01 | 0.73800 | 0.12500 | -1.17e-01 | 0.043600 | 5.01e-01 | 8.03e-01 | 
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 13 | 5.11e-01 | 0.76900 | 0.12500 | 9.54e-03 | -0.124000 | 9.53e-01 | 4.38e-01 | 
| Retrograde transport at the Trans-Golgi-Network | 42 | 9.73e-02 | 0.44100 | 0.12400 | 1.76e-02 | -0.123000 | 8.43e-01 | 1.68e-01 | 
| Mismatch Repair | 13 | 7.99e-01 | 0.91600 | 0.12400 | -6.46e-02 | -0.106000 | 6.87e-01 | 5.07e-01 | 
| Unfolded Protein Response (UPR) | 72 | 2.90e-01 | 0.62700 | 0.12300 | -6.29e-02 | -0.106000 | 3.57e-01 | 1.20e-01 | 
| Insulin receptor signalling cascade | 23 | 6.71e-01 | 0.85100 | 0.12300 | -1.06e-01 | -0.062800 | 3.78e-01 | 6.03e-01 | 
| Transcription of the HIV genome | 50 | 4.60e-01 | 0.73800 | 0.12300 | -6.82e-02 | -0.102000 | 4.05e-01 | 2.13e-01 | 
| Cap-dependent Translation Initiation | 91 | 2.39e-01 | 0.59500 | 0.12200 | -6.68e-02 | -0.103000 | 2.72e-01 | 9.16e-02 | 
| Eukaryotic Translation Initiation | 91 | 2.39e-01 | 0.59500 | 0.12200 | -6.68e-02 | -0.103000 | 2.72e-01 | 9.16e-02 | 
| FOXO-mediated transcription | 45 | 2.33e-01 | 0.59000 | 0.12200 | 2.44e-02 | 0.120000 | 7.78e-01 | 1.65e-01 | 
| Inactivation of APC/C via direct inhibition of the APC/C complex | 16 | 8.05e-01 | 0.91600 | 0.12200 | 7.82e-02 | 0.093800 | 5.88e-01 | 5.16e-01 | 
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 16 | 8.05e-01 | 0.91600 | 0.12200 | 7.82e-02 | 0.093800 | 5.88e-01 | 5.16e-01 | 
| Regulation of beta-cell development | 15 | 6.96e-01 | 0.86700 | 0.12200 | 1.14e-01 | 0.042200 | 4.43e-01 | 7.77e-01 | 
| rRNA processing | 155 | 2.63e-02 | 0.23500 | 0.12200 | -4.27e-02 | -0.114000 | 3.61e-01 | 1.47e-02 | 
| Regulation of MECP2 expression and activity | 20 | 5.62e-01 | 0.78700 | 0.12100 | 3.10e-02 | 0.117000 | 8.11e-01 | 3.64e-01 | 
| Diseases associated with the TLR signaling cascade | 15 | 7.96e-01 | 0.91600 | 0.12100 | -6.71e-02 | -0.101000 | 6.53e-01 | 5.00e-01 | 
| Diseases of Immune System | 15 | 7.96e-01 | 0.91600 | 0.12100 | -6.71e-02 | -0.101000 | 6.53e-01 | 5.00e-01 | 
| PIP3 activates AKT signaling | 172 | 9.30e-02 | 0.43300 | 0.12100 | -7.30e-02 | -0.096600 | 1.00e-01 | 2.97e-02 | 
| Toll Like Receptor 4 (TLR4) Cascade | 86 | 3.34e-01 | 0.67800 | 0.12100 | -8.48e-02 | -0.086200 | 1.75e-01 | 1.68e-01 | 
| RHOBTB2 GTPase cycle | 19 | 2.42e-01 | 0.59600 | 0.12100 | 9.03e-02 | -0.080400 | 4.96e-01 | 5.44e-01 | 
| NOTCH3 Intracellular Domain Regulates Transcription | 15 | 7.47e-01 | 0.89700 | 0.12100 | 1.09e-01 | 0.052800 | 4.66e-01 | 7.23e-01 | 
| B-WICH complex positively regulates rRNA expression | 27 | 6.41e-01 | 0.83200 | 0.12100 | 1.04e-01 | 0.061700 | 3.52e-01 | 5.79e-01 | 
| Cilium Assembly | 135 | 2.60e-02 | 0.23500 | 0.12000 | -3.27e-02 | -0.116000 | 5.13e-01 | 2.06e-02 | 
| Transport of vitamins, nucleosides, and related molecules | 19 | 7.30e-01 | 0.89100 | 0.12000 | 6.09e-02 | 0.104000 | 6.46e-01 | 4.34e-01 | 
| Signaling by Non-Receptor Tyrosine Kinases | 33 | 3.36e-01 | 0.67800 | 0.12000 | -1.18e-01 | -0.019900 | 2.40e-01 | 8.43e-01 | 
| Signaling by PTK6 | 33 | 3.36e-01 | 0.67800 | 0.12000 | -1.18e-01 | -0.019900 | 2.40e-01 | 8.43e-01 | 
| Major pathway of rRNA processing in the nucleolus and cytosol | 145 | 3.92e-02 | 0.30200 | 0.12000 | -4.31e-02 | -0.112000 | 3.72e-01 | 2.06e-02 | 
| ERKs are inactivated | 11 | 5.02e-01 | 0.76200 | 0.12000 | -1.12e-01 | 0.041000 | 5.19e-01 | 8.14e-01 | 
| Late endosomal microautophagy | 21 | 4.03e-01 | 0.71500 | 0.12000 | 1.20e-01 | -0.000834 | 3.43e-01 | 9.95e-01 | 
| Regulation of APC/C activators between G1/S and early anaphase | 64 | 4.50e-01 | 0.73200 | 0.11900 | -8.35e-02 | -0.085400 | 2.49e-01 | 2.38e-01 | 
| ERK/MAPK targets | 16 | 7.93e-01 | 0.91600 | 0.11900 | -6.78e-02 | -0.098300 | 6.39e-01 | 4.96e-01 | 
| Clathrin-mediated endocytosis | 82 | 1.85e-02 | 0.21600 | 0.11900 | 1.29e-02 | -0.118000 | 8.41e-01 | 6.44e-02 | 
| Association of TriC/CCT with target proteins during biosynthesis | 29 | 4.93e-01 | 0.75600 | 0.11900 | -1.13e-01 | -0.037300 | 2.94e-01 | 7.28e-01 | 
| PTEN Regulation | 104 | 2.72e-01 | 0.61700 | 0.11800 | -7.56e-02 | -0.090400 | 1.84e-01 | 1.12e-01 | 
| Signaling by NOTCH1 | 51 | 5.00e-01 | 0.76000 | 0.11800 | 6.90e-02 | 0.095400 | 3.95e-01 | 2.39e-01 | 
| Protein ubiquitination | 56 | 3.71e-01 | 0.71100 | 0.11800 | -1.05e-01 | -0.053300 | 1.75e-01 | 4.91e-01 | 
| rRNA processing in the nucleus and cytosol | 151 | 4.86e-02 | 0.34400 | 0.11800 | -4.60e-02 | -0.108000 | 3.31e-01 | 2.24e-02 | 
| RET signaling | 22 | 7.66e-01 | 0.90400 | 0.11700 | 8.00e-02 | 0.085600 | 5.16e-01 | 4.87e-01 | 
| Metal ion SLC transporters | 15 | 5.90e-01 | 0.80200 | 0.11700 | -1.16e-01 | -0.012100 | 4.35e-01 | 9.35e-01 | 
| PINK1-PRKN Mediated Mitophagy | 19 | 3.18e-01 | 0.66200 | 0.11700 | -4.14e-02 | 0.109000 | 7.55e-01 | 4.09e-01 | 
| DNA Replication | 100 | 3.03e-01 | 0.64600 | 0.11700 | -8.50e-02 | -0.080400 | 1.43e-01 | 1.66e-01 | 
| Synthesis of PIPs at the early endosome membrane | 12 | 6.83e-01 | 0.85700 | 0.11700 | -1.86e-02 | -0.115000 | 9.11e-01 | 4.89e-01 | 
| Downstream signaling events of B Cell Receptor (BCR) | 66 | 2.61e-01 | 0.60300 | 0.11600 | -1.08e-01 | -0.044000 | 1.31e-01 | 5.37e-01 | 
| MAP kinase activation | 46 | 5.81e-01 | 0.79800 | 0.11600 | -8.31e-02 | -0.081100 | 3.30e-01 | 3.42e-01 | 
| Cargo recognition for clathrin-mediated endocytosis | 57 | 9.10e-02 | 0.43300 | 0.11600 | 4.01e-03 | -0.116000 | 9.58e-01 | 1.31e-01 | 
| Cell surface interactions at the vascular wall | 54 | 4.06e-01 | 0.71500 | 0.11600 | 5.40e-02 | 0.102000 | 4.93e-01 | 1.93e-01 | 
| SUMOylation of intracellular receptors | 19 | 7.01e-01 | 0.86900 | 0.11500 | 4.72e-02 | 0.105000 | 7.22e-01 | 4.29e-01 | 
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 64 | 4.24e-01 | 0.71800 | 0.11500 | -9.48e-02 | -0.065000 | 1.91e-01 | 3.69e-01 | 
| Toll Like Receptor 2 (TLR2) Cascade | 64 | 4.24e-01 | 0.71800 | 0.11500 | -9.48e-02 | -0.065000 | 1.91e-01 | 3.69e-01 | 
| Toll Like Receptor TLR1:TLR2 Cascade | 64 | 4.24e-01 | 0.71800 | 0.11500 | -9.48e-02 | -0.065000 | 1.91e-01 | 3.69e-01 | 
| Toll Like Receptor TLR6:TLR2 Cascade | 64 | 4.24e-01 | 0.71800 | 0.11500 | -9.48e-02 | -0.065000 | 1.91e-01 | 3.69e-01 | 
| Regulation of KIT signaling | 10 | 8.67e-01 | 0.94300 | 0.11500 | 9.71e-02 | 0.061500 | 5.95e-01 | 7.36e-01 | 
| RNA Polymerase III Abortive And Retractive Initiation | 38 | 6.47e-01 | 0.83700 | 0.11400 | -7.98e-02 | -0.081900 | 3.95e-01 | 3.83e-01 | 
| RNA Polymerase III Transcription | 38 | 6.47e-01 | 0.83700 | 0.11400 | -7.98e-02 | -0.081900 | 3.95e-01 | 3.83e-01 | 
| Transcription of E2F targets under negative control by DREAM complex | 17 | 3.75e-01 | 0.71100 | 0.11400 | -1.07e-01 | 0.040800 | 4.46e-01 | 7.71e-01 | 
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 53 | 5.46e-01 | 0.78400 | 0.11400 | -8.20e-02 | -0.079700 | 3.03e-01 | 3.16e-01 | 
| Signaling by FGFR2 in disease | 23 | 5.49e-01 | 0.78600 | 0.11400 | -1.11e-01 | -0.027800 | 3.58e-01 | 8.17e-01 | 
| RHOD GTPase cycle | 32 | 4.75e-01 | 0.73800 | 0.11300 | 3.32e-02 | 0.108000 | 7.46e-01 | 2.89e-01 | 
| APC/C:Cdc20 mediated degradation of Cyclin B | 19 | 8.07e-01 | 0.91600 | 0.11300 | -7.90e-02 | -0.081300 | 5.51e-01 | 5.40e-01 | 
| Synthesis of DNA | 93 | 3.34e-01 | 0.67800 | 0.11300 | -7.12e-02 | -0.088100 | 2.36e-01 | 1.43e-01 | 
| HIV Infection | 175 | 1.20e-01 | 0.47100 | 0.11300 | -9.05e-02 | -0.068200 | 3.99e-02 | 1.22e-01 | 
| Metabolic disorders of biological oxidation enzymes | 13 | 8.60e-01 | 0.94100 | 0.11300 | 7.29e-02 | 0.086600 | 6.49e-01 | 5.89e-01 | 
| DNA Replication Pre-Initiation | 77 | 4.07e-01 | 0.71500 | 0.11300 | -7.18e-02 | -0.087400 | 2.77e-01 | 1.86e-01 | 
| Diseases of glycosylation | 65 | 1.52e-01 | 0.50900 | 0.11200 | 1.11e-01 | 0.018300 | 1.23e-01 | 7.99e-01 | 
| Signaling by Hedgehog | 93 | 3.08e-01 | 0.65200 | 0.11200 | -9.23e-02 | -0.063700 | 1.25e-01 | 2.90e-01 | 
| G1/S Transition | 103 | 2.70e-01 | 0.61600 | 0.11200 | -9.24e-02 | -0.063300 | 1.06e-01 | 2.68e-01 | 
| Ovarian tumor domain proteases | 29 | 7.22e-01 | 0.88700 | 0.11200 | -7.37e-02 | -0.084300 | 4.92e-01 | 4.32e-01 | 
| Cell recruitment (pro-inflammatory response) | 15 | 6.26e-01 | 0.82400 | 0.11200 | 1.29e-02 | 0.111000 | 9.31e-01 | 4.57e-01 | 
| Purinergic signaling in leishmaniasis infection | 15 | 6.26e-01 | 0.82400 | 0.11200 | 1.29e-02 | 0.111000 | 9.31e-01 | 4.57e-01 | 
| Glycosaminoglycan metabolism | 60 | 3.99e-01 | 0.71200 | 0.11200 | 9.84e-02 | 0.052500 | 1.88e-01 | 4.82e-01 | 
| RHOBTB1 GTPase cycle | 18 | 7.95e-01 | 0.91600 | 0.11100 | 6.20e-02 | 0.092200 | 6.49e-01 | 4.99e-01 | 
| Toll-like Receptor Cascades | 96 | 3.11e-01 | 0.65400 | 0.11100 | -9.05e-02 | -0.064400 | 1.27e-01 | 2.77e-01 | 
| Heme biosynthesis | 10 | 8.38e-01 | 0.93000 | 0.11100 | -4.45e-02 | -0.102000 | 8.07e-01 | 5.78e-01 | 
| IRS-mediated signalling | 19 | 5.34e-01 | 0.77400 | 0.11000 | -1.10e-01 | -0.006800 | 4.08e-01 | 9.59e-01 | 
| HIV Transcription Initiation | 36 | 5.31e-01 | 0.77400 | 0.11000 | -4.33e-02 | -0.101000 | 6.53e-01 | 2.95e-01 | 
| RNA Polymerase II HIV Promoter Escape | 36 | 5.31e-01 | 0.77400 | 0.11000 | -4.33e-02 | -0.101000 | 6.53e-01 | 2.95e-01 | 
| RNA Polymerase II Promoter Escape | 36 | 5.31e-01 | 0.77400 | 0.11000 | -4.33e-02 | -0.101000 | 6.53e-01 | 2.95e-01 | 
| RNA Polymerase II Transcription Initiation | 36 | 5.31e-01 | 0.77400 | 0.11000 | -4.33e-02 | -0.101000 | 6.53e-01 | 2.95e-01 | 
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 36 | 5.31e-01 | 0.77400 | 0.11000 | -4.33e-02 | -0.101000 | 6.53e-01 | 2.95e-01 | 
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 36 | 5.31e-01 | 0.77400 | 0.11000 | -4.33e-02 | -0.101000 | 6.53e-01 | 2.95e-01 | 
| NR1H2 and NR1H3-mediated signaling | 24 | 7.75e-01 | 0.90900 | 0.10900 | 8.11e-02 | 0.073300 | 4.92e-01 | 5.35e-01 | 
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 84 | 4.00e-01 | 0.71200 | 0.10900 | -8.49e-02 | -0.067900 | 1.79e-01 | 2.83e-01 | 
| Nonsense-Mediated Decay (NMD) | 84 | 4.00e-01 | 0.71200 | 0.10900 | -8.49e-02 | -0.067900 | 1.79e-01 | 2.83e-01 | 
| Response of EIF2AK1 (HRI) to heme deficiency | 13 | 8.64e-01 | 0.94200 | 0.10900 | 8.64e-02 | 0.065800 | 5.90e-01 | 6.81e-01 | 
| CTLA4 inhibitory signaling | 15 | 8.47e-01 | 0.93600 | 0.10900 | 6.68e-02 | 0.085600 | 6.54e-01 | 5.66e-01 | 
| DAP12 interactions | 19 | 7.26e-01 | 0.89000 | 0.10800 | -9.93e-02 | -0.043700 | 4.54e-01 | 7.42e-01 | 
| Constitutive Signaling by Aberrant PI3K in Cancer | 27 | 6.97e-01 | 0.86700 | 0.10800 | -5.50e-02 | -0.093300 | 6.21e-01 | 4.02e-01 | 
| RHOC GTPase cycle | 45 | 1.06e-01 | 0.45800 | 0.10800 | -1.03e-01 | 0.033800 | 2.33e-01 | 6.95e-01 | 
| Fanconi Anemia Pathway | 28 | 2.89e-01 | 0.62700 | 0.10800 | 2.13e-02 | -0.106000 | 8.45e-01 | 3.34e-01 | 
| RNA Polymerase I Transcription Initiation | 39 | 5.29e-01 | 0.77400 | 0.10800 | 9.82e-02 | 0.044100 | 2.89e-01 | 6.34e-01 | 
| Nuclear events mediated by NFE2L2 | 63 | 1.75e-01 | 0.51400 | 0.10700 | -1.06e-01 | -0.014500 | 1.46e-01 | 8.42e-01 | 
| Dual Incision in GG-NER | 34 | 4.74e-01 | 0.73800 | 0.10700 | -2.82e-02 | -0.103000 | 7.76e-01 | 2.98e-01 | 
| Signaling by ERBB2 | 33 | 5.84e-01 | 0.79900 | 0.10700 | -4.33e-02 | -0.097800 | 6.67e-01 | 3.31e-01 | 
| Role of phospholipids in phagocytosis | 14 | 4.66e-01 | 0.73800 | 0.10600 | 9.30e-02 | -0.051900 | 5.47e-01 | 7.37e-01 | 
| Signaling by FLT3 fusion proteins | 15 | 5.86e-01 | 0.79900 | 0.10600 | -4.55e-03 | 0.106000 | 9.76e-01 | 4.78e-01 | 
| Fatty acid metabolism | 90 | 4.14e-01 | 0.71800 | 0.10600 | 7.68e-02 | 0.072900 | 2.09e-01 | 2.33e-01 | 
| G1/S-Specific Transcription | 23 | 4.68e-01 | 0.73800 | 0.10600 | 1.20e-03 | 0.106000 | 9.92e-01 | 3.80e-01 | 
| Amino acid transport across the plasma membrane | 15 | 8.21e-01 | 0.92100 | 0.10600 | 9.19e-02 | 0.052300 | 5.38e-01 | 7.26e-01 | 
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 15 | 6.20e-01 | 0.82400 | 0.10600 | -3.60e-03 | -0.106000 | 9.81e-01 | 4.79e-01 | 
| Nicotinate metabolism | 16 | 8.04e-01 | 0.91600 | 0.10600 | 5.03e-02 | 0.092900 | 7.27e-01 | 5.20e-01 | 
| TP53 Regulates Metabolic Genes | 61 | 5.28e-01 | 0.77400 | 0.10500 | -6.43e-02 | -0.083500 | 3.86e-01 | 2.60e-01 | 
| Signaling by FGFR in disease | 38 | 2.03e-01 | 0.55100 | 0.10500 | -1.03e-01 | 0.020500 | 2.72e-01 | 8.27e-01 | 
| SUMOylation of chromatin organization proteins | 45 | 2.29e-01 | 0.58800 | 0.10500 | -1.05e-01 | -0.000427 | 2.23e-01 | 9.96e-01 | 
| Transcriptional Regulation by TP53 | 272 | 7.57e-02 | 0.40400 | 0.10500 | -7.14e-02 | -0.077000 | 4.43e-02 | 3.00e-02 | 
| TRAF6 mediated IRF7 activation | 16 | 4.20e-01 | 0.71800 | 0.10500 | -5.79e-02 | 0.087100 | 6.89e-01 | 5.47e-01 | 
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 15 | 7.39e-01 | 0.89100 | 0.10400 | 1.00e-01 | 0.029200 | 5.03e-01 | 8.45e-01 | 
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 15 | 7.39e-01 | 0.89100 | 0.10400 | 1.00e-01 | 0.029200 | 5.03e-01 | 8.45e-01 | 
| Plasma lipoprotein assembly, remodeling, and clearance | 35 | 4.87e-01 | 0.75100 | 0.10300 | -2.63e-02 | -0.099300 | 7.88e-01 | 3.10e-01 | 
| Switching of origins to a post-replicative state | 69 | 5.29e-01 | 0.77400 | 0.10200 | -7.57e-02 | -0.068800 | 2.78e-01 | 3.24e-01 | 
| Oxidative Stress Induced Senescence | 51 | 4.80e-01 | 0.74100 | 0.10200 | -4.27e-02 | -0.092800 | 5.98e-01 | 2.52e-01 | 
| Translation of Replicase and Assembly of the Replication Transcription Complex | 10 | 8.82e-01 | 0.94900 | 0.10200 | 8.94e-02 | 0.049300 | 6.25e-01 | 7.87e-01 | 
| Gap-filling DNA repair synthesis and ligation in TC-NER | 54 | 1.74e-01 | 0.51400 | 0.10200 | 2.88e-03 | -0.102000 | 9.71e-01 | 1.95e-01 | 
| Golgi Associated Vesicle Biogenesis | 37 | 2.54e-01 | 0.60000 | 0.10200 | 1.01e-01 | -0.014600 | 2.90e-01 | 8.78e-01 | 
| RNA polymerase II transcribes snRNA genes | 65 | 5.59e-01 | 0.78700 | 0.10100 | -7.31e-02 | -0.069900 | 3.09e-01 | 3.31e-01 | 
| MTOR signalling | 32 | 5.11e-01 | 0.76900 | 0.10100 | 9.84e-02 | 0.022800 | 3.36e-01 | 8.23e-01 | 
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 28 | 2.69e-01 | 0.61600 | 0.10100 | -9.16e-02 | 0.042300 | 4.02e-01 | 6.99e-01 | 
| L13a-mediated translational silencing of Ceruloplasmin expression | 83 | 2.77e-01 | 0.62000 | 0.10100 | -3.76e-02 | -0.093600 | 5.55e-01 | 1.41e-01 | 
| Toll Like Receptor 3 (TLR3) Cascade | 71 | 5.37e-01 | 0.77500 | 0.10000 | -6.95e-02 | -0.072100 | 3.12e-01 | 2.94e-01 | 
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 13 | 7.39e-01 | 0.89100 | 0.10000 | -1.62e-02 | -0.098700 | 9.19e-01 | 5.38e-01 | 
| Listeria monocytogenes entry into host cells | 14 | 7.62e-01 | 0.90200 | 0.09980 | -2.54e-02 | -0.096500 | 8.69e-01 | 5.32e-01 | 
| Prefoldin mediated transfer of substrate to CCT/TriC | 16 | 8.25e-01 | 0.92300 | 0.09950 | -8.73e-02 | -0.047700 | 5.45e-01 | 7.41e-01 | 
| NOTCH4 Intracellular Domain Regulates Transcription | 14 | 5.32e-01 | 0.77400 | 0.09950 | 3.96e-02 | -0.091300 | 7.98e-01 | 5.54e-01 | 
| RNA Polymerase I Promoter Escape | 26 | 7.98e-01 | 0.91600 | 0.09880 | 7.39e-02 | 0.065500 | 5.15e-01 | 5.63e-01 | 
| Chromatin modifying enzymes | 139 | 9.30e-02 | 0.43300 | 0.09870 | -9.41e-02 | -0.029800 | 5.65e-02 | 5.46e-01 | 
| Chromatin organization | 139 | 9.30e-02 | 0.43300 | 0.09870 | -9.41e-02 | -0.029800 | 5.65e-02 | 5.46e-01 | 
| Pyruvate metabolism and Citric Acid (TCA) cycle | 38 | 3.63e-01 | 0.70500 | 0.09840 | -9.82e-02 | -0.005460 | 2.95e-01 | 9.54e-01 | 
| RHO GTPases activate PKNs | 26 | 6.77e-01 | 0.85300 | 0.09820 | -3.59e-02 | -0.091400 | 7.51e-01 | 4.20e-01 | 
| Downstream signal transduction | 20 | 5.18e-01 | 0.77400 | 0.09790 | -9.95e-03 | 0.097400 | 9.39e-01 | 4.51e-01 | 
| C-type lectin receptors (CLRs) | 92 | 4.17e-01 | 0.71800 | 0.09760 | -8.00e-02 | -0.055900 | 1.86e-01 | 3.55e-01 | 
| S Phase | 127 | 3.49e-01 | 0.69200 | 0.09710 | -7.21e-02 | -0.065100 | 1.62e-01 | 2.07e-01 | 
| trans-Golgi Network Vesicle Budding | 50 | 9.67e-02 | 0.44100 | 0.09650 | 7.70e-02 | -0.058100 | 3.47e-01 | 4.78e-01 | 
| Activation of ATR in response to replication stress | 29 | 5.35e-01 | 0.77400 | 0.09640 | -1.54e-02 | -0.095100 | 8.86e-01 | 3.76e-01 | 
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 29 | 7.33e-01 | 0.89100 | 0.09630 | 8.33e-02 | 0.048300 | 4.38e-01 | 6.52e-01 | 
| Formation of a pool of free 40S subunits | 75 | 3.28e-01 | 0.67400 | 0.09580 | -3.30e-02 | -0.089900 | 6.22e-01 | 1.79e-01 | 
| RAF-independent MAPK1/3 activation | 19 | 7.67e-01 | 0.90400 | 0.09580 | 3.58e-02 | 0.088800 | 7.87e-01 | 5.03e-01 | 
| Glycolysis | 54 | 3.05e-01 | 0.64800 | 0.09540 | -9.45e-02 | -0.013100 | 2.30e-01 | 8.68e-01 | 
| Regulation of actin dynamics for phagocytic cup formation | 42 | 6.10e-01 | 0.81700 | 0.09500 | -8.51e-02 | -0.042300 | 3.41e-01 | 6.36e-01 | 
| GTP hydrolysis and joining of the 60S ribosomal subunit | 84 | 3.52e-01 | 0.69300 | 0.09490 | -3.96e-02 | -0.086300 | 5.31e-01 | 1.73e-01 | 
| Peptide chain elongation | 67 | 5.90e-01 | 0.80200 | 0.09480 | -6.54e-02 | -0.068700 | 3.56e-01 | 3.32e-01 | 
| Eukaryotic Translation Elongation | 70 | 5.64e-01 | 0.78800 | 0.09470 | -7.31e-02 | -0.060300 | 2.91e-01 | 3.84e-01 | 
| RHOB GTPase cycle | 40 | 4.91e-01 | 0.75200 | 0.09460 | -9.17e-02 | -0.023000 | 3.16e-01 | 8.01e-01 | 
| MET promotes cell motility | 11 | 9.17e-01 | 0.96500 | 0.09400 | 6.32e-02 | 0.069600 | 7.17e-01 | 6.89e-01 | 
| Gamma carboxylation, hypusine formation and arylsulfatase activation | 21 | 8.31e-01 | 0.92400 | 0.09390 | 7.68e-02 | 0.054100 | 5.43e-01 | 6.68e-01 | 
| Mitophagy | 23 | 4.53e-01 | 0.73200 | 0.09310 | -2.21e-02 | 0.090400 | 8.55e-01 | 4.53e-01 | 
| O-linked glycosylation of mucins | 24 | 6.16e-01 | 0.82200 | 0.09190 | 9.10e-02 | 0.013300 | 4.41e-01 | 9.11e-01 | 
| Apoptosis | 124 | 4.08e-01 | 0.71500 | 0.09130 | -6.44e-02 | -0.064700 | 2.17e-01 | 2.15e-01 | 
| RND2 GTPase cycle | 33 | 7.86e-01 | 0.91600 | 0.09110 | 6.33e-02 | 0.065500 | 5.29e-01 | 5.15e-01 | 
| RNA Pol II CTD phosphorylation and interaction with CE | 23 | 4.25e-01 | 0.71800 | 0.09070 | 8.35e-02 | -0.035500 | 4.89e-01 | 7.68e-01 | 
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 23 | 4.25e-01 | 0.71800 | 0.09070 | 8.35e-02 | -0.035500 | 4.89e-01 | 7.68e-01 | 
| NOTCH1 Intracellular Domain Regulates Transcription | 37 | 6.93e-01 | 0.86700 | 0.09070 | 4.36e-02 | 0.079500 | 6.47e-01 | 4.03e-01 | 
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 59 | 5.97e-01 | 0.80300 | 0.09060 | -4.90e-02 | -0.076200 | 5.16e-01 | 3.12e-01 | 
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 15 | 7.55e-01 | 0.89800 | 0.09050 | -1.55e-02 | -0.089200 | 9.17e-01 | 5.50e-01 | 
| Organelle biogenesis and maintenance | 187 | 4.09e-02 | 0.31000 | 0.08960 | -1.80e-02 | -0.087800 | 6.73e-01 | 3.94e-02 | 
| E2F mediated regulation of DNA replication | 12 | 7.72e-01 | 0.90700 | 0.08930 | 8.91e-02 | 0.006300 | 5.93e-01 | 9.70e-01 | 
| Mitochondrial protein import | 40 | 2.46e-01 | 0.59600 | 0.08900 | 3.23e-02 | -0.082900 | 7.24e-01 | 3.65e-01 | 
| Late Phase of HIV Life Cycle | 106 | 4.76e-01 | 0.73800 | 0.08850 | -6.72e-02 | -0.057500 | 2.33e-01 | 3.08e-01 | 
| Intracellular signaling by second messengers | 194 | 1.44e-01 | 0.49200 | 0.08790 | -3.88e-02 | -0.078800 | 3.54e-01 | 5.97e-02 | 
| RND1 GTPase cycle | 29 | 5.42e-01 | 0.77900 | 0.08790 | 5.39e-03 | 0.087700 | 9.60e-01 | 4.14e-01 | 
| HIV Life Cycle | 117 | 4.45e-01 | 0.73100 | 0.08790 | -6.70e-02 | -0.056800 | 2.12e-01 | 2.90e-01 | 
| RHOV GTPase cycle | 25 | 6.36e-01 | 0.83000 | 0.08770 | 1.35e-02 | 0.086700 | 9.07e-01 | 4.53e-01 | 
| The NLRP3 inflammasome | 12 | 8.48e-01 | 0.93600 | 0.08730 | 8.35e-02 | 0.025700 | 6.17e-01 | 8.78e-01 | 
| Mitotic G1 phase and G1/S transition | 118 | 3.97e-01 | 0.71200 | 0.08730 | -7.25e-02 | -0.048500 | 1.75e-01 | 3.64e-01 | 
| SUMO E3 ligases SUMOylate target proteins | 127 | 4.35e-01 | 0.72400 | 0.08690 | -6.26e-02 | -0.060300 | 2.25e-01 | 2.42e-01 | 
| Eukaryotic Translation Termination | 70 | 6.27e-01 | 0.82400 | 0.08680 | -6.47e-02 | -0.057900 | 3.50e-01 | 4.03e-01 | 
| RHO GTPases Activate WASPs and WAVEs | 28 | 8.30e-01 | 0.92400 | 0.08670 | -6.44e-02 | -0.058100 | 5.55e-01 | 5.95e-01 | 
| Elastic fibre formation | 13 | 7.56e-01 | 0.89800 | 0.08670 | 8.66e-02 | 0.002630 | 5.89e-01 | 9.87e-01 | 
| KEAP1-NFE2L2 pathway | 81 | 2.58e-01 | 0.60300 | 0.08650 | -8.51e-02 | -0.015500 | 1.86e-01 | 8.09e-01 | 
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 12 | 7.66e-01 | 0.90400 | 0.08640 | -3.90e-04 | -0.086400 | 9.98e-01 | 6.04e-01 | 
| Signaling by PDGF | 24 | 4.14e-01 | 0.71700 | 0.08620 | -4.77e-02 | 0.071800 | 6.86e-01 | 5.43e-01 | 
| Potential therapeutics for SARS | 63 | 2.70e-01 | 0.61600 | 0.08620 | -8.61e-02 | -0.003800 | 2.38e-01 | 9.58e-01 | 
| TP53 Regulates Transcription of Cell Cycle Genes | 40 | 7.36e-01 | 0.89100 | 0.08590 | -4.76e-02 | -0.071600 | 6.03e-01 | 4.34e-01 | 
| Mitochondrial Fatty Acid Beta-Oxidation | 25 | 7.18e-01 | 0.88400 | 0.08590 | 8.20e-02 | 0.025400 | 4.78e-01 | 8.26e-01 | 
| Degradation of beta-catenin by the destruction complex | 64 | 6.24e-01 | 0.82400 | 0.08590 | -7.03e-02 | -0.049300 | 3.31e-01 | 4.96e-01 | 
| Positive epigenetic regulation of rRNA expression | 40 | 6.45e-01 | 0.83600 | 0.08580 | 7.92e-02 | 0.032900 | 3.87e-01 | 7.19e-01 | 
| Protein methylation | 10 | 7.01e-01 | 0.86900 | 0.08550 | 4.33e-02 | -0.073700 | 8.13e-01 | 6.86e-01 | 
| GPER1 signaling | 20 | 8.79e-01 | 0.94900 | 0.08490 | 6.41e-02 | 0.055700 | 6.20e-01 | 6.66e-01 | 
| Signaling by the B Cell Receptor (BCR) | 84 | 3.70e-01 | 0.71100 | 0.08490 | -8.00e-02 | -0.028500 | 2.06e-01 | 6.52e-01 | 
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 20 | 8.83e-01 | 0.94900 | 0.08440 | 5.90e-02 | 0.060400 | 6.48e-01 | 6.40e-01 | 
| Nuclear signaling by ERBB4 | 14 | 8.07e-01 | 0.91600 | 0.08340 | 1.61e-02 | 0.081900 | 9.17e-01 | 5.96e-01 | 
| FCGR3A-mediated phagocytosis | 40 | 6.79e-01 | 0.85300 | 0.08330 | -7.58e-02 | -0.034500 | 4.07e-01 | 7.06e-01 | 
| Leishmania phagocytosis | 40 | 6.79e-01 | 0.85300 | 0.08330 | -7.58e-02 | -0.034500 | 4.07e-01 | 7.06e-01 | 
| Parasite infection | 40 | 6.79e-01 | 0.85300 | 0.08330 | -7.58e-02 | -0.034500 | 4.07e-01 | 7.06e-01 | 
| Polo-like kinase mediated events | 16 | 6.00e-01 | 0.80500 | 0.08320 | -3.47e-02 | 0.075600 | 8.10e-01 | 6.01e-01 | 
| Signaling by VEGF | 72 | 4.17e-01 | 0.71800 | 0.08290 | 7.90e-02 | 0.024900 | 2.47e-01 | 7.15e-01 | 
| Signaling by NTRK1 (TRKA) | 79 | 1.39e-01 | 0.49100 | 0.08270 | -8.16e-02 | 0.013400 | 2.11e-01 | 8.38e-01 | 
| Mitochondrial iron-sulfur cluster biogenesis | 12 | 6.96e-01 | 0.86700 | 0.08270 | 2.96e-02 | -0.077200 | 8.59e-01 | 6.44e-01 | 
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 19 | 8.91e-01 | 0.95200 | 0.08260 | 5.55e-02 | 0.061200 | 6.76e-01 | 6.44e-01 | 
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | 11 | 8.82e-01 | 0.94900 | 0.08230 | 7.78e-02 | 0.026900 | 6.55e-01 | 8.77e-01 | 
| Dual incision in TC-NER | 55 | 1.54e-01 | 0.51200 | 0.08220 | 5.06e-02 | -0.064900 | 5.17e-01 | 4.06e-01 | 
| Signaling by NOTCH2 | 18 | 7.59e-01 | 0.90000 | 0.08210 | -1.42e-02 | -0.080900 | 9.17e-01 | 5.53e-01 | 
| GPVI-mediated activation cascade | 21 | 8.60e-01 | 0.94100 | 0.08190 | -4.41e-02 | -0.069000 | 7.26e-01 | 5.84e-01 | 
| Protein localization | 110 | 3.86e-01 | 0.71200 | 0.08180 | -3.64e-02 | -0.073200 | 5.11e-01 | 1.86e-01 | 
| mTORC1-mediated signalling | 17 | 9.04e-01 | 0.95600 | 0.08170 | -6.02e-02 | -0.055300 | 6.68e-01 | 6.93e-01 | 
| Metabolism of nucleotides | 64 | 3.98e-01 | 0.71200 | 0.08170 | -8.00e-02 | -0.016300 | 2.69e-01 | 8.22e-01 | 
| EPHB-mediated forward signaling | 25 | 8.64e-01 | 0.94200 | 0.08160 | -5.77e-02 | -0.057800 | 6.18e-01 | 6.17e-01 | 
| IRS-related events triggered by IGF1R | 20 | 7.09e-01 | 0.87800 | 0.08110 | -8.08e-02 | -0.007380 | 5.32e-01 | 9.54e-01 | 
| VEGFA-VEGFR2 Pathway | 70 | 4.28e-01 | 0.71900 | 0.08110 | 7.78e-02 | 0.022800 | 2.61e-01 | 7.42e-01 | 
| Iron uptake and transport | 36 | 6.38e-01 | 0.83100 | 0.08100 | -7.81e-02 | -0.021700 | 4.18e-01 | 8.22e-01 | 
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 49 | 7.52e-01 | 0.89700 | 0.08020 | -5.16e-02 | -0.061400 | 5.33e-01 | 4.58e-01 | 
| Apoptotic execution phase | 30 | 4.32e-01 | 0.72100 | 0.08020 | 2.75e-02 | -0.075300 | 7.95e-01 | 4.76e-01 | 
| Costimulation by the CD28 family | 41 | 5.81e-01 | 0.79800 | 0.07990 | 1.77e-02 | 0.077900 | 8.45e-01 | 3.88e-01 | 
| Fc epsilon receptor (FCERI) signaling | 100 | 3.93e-01 | 0.71200 | 0.07990 | -7.36e-02 | -0.031100 | 2.05e-01 | 5.92e-01 | 
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 18 | 8.60e-01 | 0.94100 | 0.07980 | 3.52e-02 | 0.071700 | 7.96e-01 | 5.99e-01 | 
| Formation of TC-NER Pre-Incision Complex | 45 | 3.76e-01 | 0.71100 | 0.07970 | 7.92e-02 | -0.008320 | 3.59e-01 | 9.23e-01 | 
| ECM proteoglycans | 10 | 7.53e-01 | 0.89700 | 0.07960 | 7.38e-02 | -0.029900 | 6.86e-01 | 8.70e-01 | 
| Cellular response to starvation | 110 | 5.49e-01 | 0.78600 | 0.07920 | -5.70e-02 | -0.054900 | 3.03e-01 | 3.21e-01 | 
| G0 and Early G1 | 24 | 4.64e-01 | 0.73800 | 0.07920 | -5.89e-02 | 0.052900 | 6.18e-01 | 6.54e-01 | 
| Programmed Cell Death | 144 | 4.28e-01 | 0.71900 | 0.07910 | -4.78e-02 | -0.063000 | 3.24e-01 | 1.94e-01 | 
| Intrinsic Pathway for Apoptosis | 43 | 4.89e-01 | 0.75200 | 0.07880 | 5.93e-03 | 0.078600 | 9.46e-01 | 3.73e-01 | 
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 10 | 8.45e-01 | 0.93600 | 0.07880 | -5.52e-03 | -0.078600 | 9.76e-01 | 6.67e-01 | 
| EPH-ephrin mediated repulsion of cells | 24 | 8.02e-01 | 0.91600 | 0.07880 | 7.26e-02 | 0.030500 | 5.38e-01 | 7.96e-01 | 
| TNFR1-induced NFkappaB signaling pathway | 19 | 7.39e-01 | 0.89100 | 0.07840 | -7.59e-03 | -0.078000 | 9.54e-01 | 5.56e-01 | 
| Cytokine Signaling in Immune system | 392 | 6.54e-02 | 0.37900 | 0.07830 | -6.81e-02 | -0.038500 | 2.20e-02 | 1.96e-01 | 
| Synthesis of substrates in N-glycan biosythesis | 46 | 7.59e-01 | 0.90000 | 0.07810 | -4.58e-02 | -0.063300 | 5.92e-01 | 4.58e-01 | 
| Infectious disease | 591 | 4.86e-02 | 0.34400 | 0.07780 | -5.87e-02 | -0.051100 | 1.66e-02 | 3.70e-02 | 
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 27 | 8.28e-01 | 0.92300 | 0.07720 | -3.84e-02 | -0.067100 | 7.30e-01 | 5.47e-01 | 
| Sema3A PAK dependent Axon repulsion | 10 | 9.48e-01 | 0.97300 | 0.07680 | -5.82e-02 | -0.050100 | 7.50e-01 | 7.84e-01 | 
| Transcriptional Regulation by E2F6 | 26 | 6.70e-01 | 0.85100 | 0.07630 | -7.60e-02 | -0.006260 | 5.02e-01 | 9.56e-01 | 
| Cellular responses to stimuli | 513 | 8.32e-02 | 0.41900 | 0.07630 | -5.36e-02 | -0.054200 | 4.05e-02 | 3.83e-02 | 
| RHOBTB GTPase Cycle | 28 | 5.84e-01 | 0.79900 | 0.07610 | 5.71e-03 | -0.075900 | 9.58e-01 | 4.87e-01 | 
| Transcriptional regulation by RUNX2 | 78 | 6.23e-01 | 0.82400 | 0.07580 | -6.37e-02 | -0.041200 | 3.32e-01 | 5.30e-01 | 
| CD28 co-stimulation | 27 | 7.99e-01 | 0.91600 | 0.07530 | 6.93e-02 | 0.029700 | 5.34e-01 | 7.90e-01 | 
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 12 | 9.42e-01 | 0.97300 | 0.07530 | 5.21e-02 | 0.054300 | 7.55e-01 | 7.45e-01 | 
| Trafficking of AMPA receptors | 12 | 9.42e-01 | 0.97300 | 0.07530 | 5.21e-02 | 0.054300 | 7.55e-01 | 7.45e-01 | 
| Signaling by TGFB family members | 81 | 9.77e-02 | 0.44100 | 0.07520 | -5.46e-02 | 0.051700 | 3.97e-01 | 4.22e-01 | 
| Synthesis of PIPs at the plasma membrane | 34 | 8.44e-01 | 0.93600 | 0.07500 | 5.07e-02 | 0.055300 | 6.10e-01 | 5.77e-01 | 
| Cellular responses to stress | 509 | 9.26e-02 | 0.43300 | 0.07490 | -5.31e-02 | -0.052800 | 4.31e-02 | 4.46e-02 | 
| Viral mRNA Translation | 67 | 7.21e-01 | 0.88600 | 0.07480 | -5.26e-02 | -0.053100 | 4.57e-01 | 4.53e-01 | 
| Signaling by ERBB2 KD Mutants | 12 | 7.90e-01 | 0.91600 | 0.07450 | -9.39e-03 | 0.073900 | 9.55e-01 | 6.58e-01 | 
| APC-Cdc20 mediated degradation of Nek2A | 21 | 8.77e-01 | 0.94900 | 0.07450 | -6.39e-02 | -0.038200 | 6.12e-01 | 7.62e-01 | 
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 72 | 6.70e-01 | 0.85100 | 0.07440 | -6.11e-02 | -0.042500 | 3.71e-01 | 5.34e-01 | 
| Nuclear Envelope (NE) Reassembly | 56 | 3.25e-01 | 0.66800 | 0.07430 | -7.34e-02 | 0.011600 | 3.43e-01 | 8.81e-01 | 
| NCAM signaling for neurite out-growth | 21 | 7.75e-01 | 0.90900 | 0.07420 | 7.28e-02 | 0.014000 | 5.64e-01 | 9.11e-01 | 
| TCR signaling | 77 | 5.69e-01 | 0.79000 | 0.07350 | -6.66e-02 | -0.031300 | 3.14e-01 | 6.36e-01 | 
| Vesicle-mediated transport | 416 | 9.02e-04 | 0.05960 | 0.07350 | 4.35e-03 | -0.073400 | 8.80e-01 | 1.12e-02 | 
| Neddylation | 175 | 2.27e-01 | 0.58700 | 0.07340 | -6.87e-02 | -0.025900 | 1.19e-01 | 5.56e-01 | 
| RNA Polymerase I Promoter Clearance | 43 | 7.17e-01 | 0.88300 | 0.07320 | 6.71e-02 | 0.029100 | 4.47e-01 | 7.42e-01 | 
| RNA Polymerase I Transcription | 43 | 7.17e-01 | 0.88300 | 0.07320 | 6.71e-02 | 0.029100 | 4.47e-01 | 7.42e-01 | 
| Stimuli-sensing channels | 35 | 6.21e-01 | 0.82400 | 0.07300 | 7.26e-02 | 0.007550 | 4.58e-01 | 9.38e-01 | 
| FOXO-mediated transcription of cell cycle genes | 12 | 9.14e-01 | 0.96300 | 0.07290 | 2.98e-02 | 0.066600 | 8.58e-01 | 6.90e-01 | 
| Metabolism of lipids | 401 | 6.57e-02 | 0.37900 | 0.07290 | 6.56e-02 | 0.031900 | 2.59e-02 | 2.79e-01 | 
| Signaling by NTRK2 (TRKB) | 15 | 7.55e-01 | 0.89800 | 0.07240 | -7.17e-02 | 0.009960 | 6.31e-01 | 9.47e-01 | 
| RHOH GTPase cycle | 25 | 5.25e-01 | 0.77400 | 0.07140 | -4.44e-02 | 0.055800 | 7.01e-01 | 6.29e-01 | 
| SARS-CoV-1 Infection | 44 | 5.87e-01 | 0.80000 | 0.07130 | -1.04e-02 | -0.070500 | 9.05e-01 | 4.19e-01 | 
| Activation of the pre-replicative complex | 23 | 7.70e-01 | 0.90600 | 0.07100 | 6.99e-02 | 0.012600 | 5.62e-01 | 9.17e-01 | 
| Transport of small molecules | 320 | 1.02e-01 | 0.45000 | 0.07090 | 6.52e-02 | 0.027800 | 4.68e-02 | 3.96e-01 | 
| Senescence-Associated Secretory Phenotype (SASP) | 39 | 5.96e-01 | 0.80300 | 0.07090 | -7.06e-02 | -0.005970 | 4.46e-01 | 9.49e-01 | 
| Sealing of the nuclear envelope (NE) by ESCRT-III | 16 | 6.63e-01 | 0.84800 | 0.07080 | -4.93e-02 | 0.050800 | 7.33e-01 | 7.25e-01 | 
| Interleukin-37 signaling | 15 | 8.03e-01 | 0.91600 | 0.07040 | 7.04e-02 | 0.000604 | 6.37e-01 | 9.97e-01 | 
| SLC transporter disorders | 48 | 8.00e-01 | 0.91600 | 0.07030 | -4.29e-02 | -0.055700 | 6.08e-01 | 5.05e-01 | 
| Membrane Trafficking | 409 | 1.62e-03 | 0.07500 | 0.07000 | 5.68e-03 | -0.069700 | 8.46e-01 | 1.68e-02 | 
| PERK regulates gene expression | 26 | 6.35e-01 | 0.83000 | 0.06980 | 9.77e-03 | -0.069200 | 9.31e-01 | 5.42e-01 | 
| Hedgehog ‘on’ state | 60 | 6.37e-01 | 0.83000 | 0.06980 | -6.50e-02 | -0.025600 | 3.85e-01 | 7.32e-01 | 
| Sialic acid metabolism | 22 | 8.75e-01 | 0.94900 | 0.06980 | 6.18e-02 | 0.032500 | 6.16e-01 | 7.92e-01 | 
| Negative regulation of the PI3K/AKT network | 54 | 7.86e-01 | 0.91600 | 0.06960 | -4.37e-02 | -0.054200 | 5.79e-01 | 4.92e-01 | 
| Cell death signalling via NRAGE, NRIF and NADE | 39 | 6.84e-01 | 0.85700 | 0.06930 | -6.74e-02 | -0.016200 | 4.67e-01 | 8.61e-01 | 
| Signaling by NTRKs | 86 | 1.86e-01 | 0.53200 | 0.06910 | -6.63e-02 | 0.019300 | 2.89e-01 | 7.58e-01 | 
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 68 | 2.00e-01 | 0.55000 | 0.06830 | 4.49e-02 | -0.051500 | 5.23e-01 | 4.64e-01 | 
| Signaling by WNT | 165 | 4.47e-01 | 0.73200 | 0.06820 | 5.73e-02 | 0.037100 | 2.06e-01 | 4.13e-01 | 
| Cellular Senescence | 99 | 5.61e-01 | 0.78700 | 0.06790 | -3.09e-02 | -0.060400 | 5.96e-01 | 3.00e-01 | 
| Metabolism of vitamins and cofactors | 103 | 4.90e-01 | 0.75200 | 0.06780 | -2.55e-02 | -0.062800 | 6.56e-01 | 2.72e-01 | 
| Platelet sensitization by LDL | 13 | 7.48e-01 | 0.89700 | 0.06740 | -5.69e-02 | 0.036100 | 7.22e-01 | 8.22e-01 | 
| The role of Nef in HIV-1 replication and disease pathogenesis | 18 | 7.63e-01 | 0.90300 | 0.06740 | -5.02e-03 | 0.067200 | 9.71e-01 | 6.22e-01 | 
| Diseases of programmed cell death | 37 | 4.51e-01 | 0.73200 | 0.06690 | 5.83e-02 | -0.032900 | 5.40e-01 | 7.29e-01 | 
| Transferrin endocytosis and recycling | 19 | 8.64e-01 | 0.94200 | 0.06640 | 6.31e-02 | 0.020700 | 6.34e-01 | 8.76e-01 | 
| Metabolism of steroids | 80 | 4.35e-01 | 0.72400 | 0.06630 | -9.78e-03 | -0.065600 | 8.80e-01 | 3.12e-01 | 
| Regulation of TP53 Activity through Acetylation | 26 | 6.56e-01 | 0.84500 | 0.06610 | 6.51e-02 | -0.011400 | 5.66e-01 | 9.20e-01 | 
| CD28 dependent PI3K/Akt signaling | 18 | 6.76e-01 | 0.85300 | 0.06610 | 5.42e-02 | -0.037700 | 6.90e-01 | 7.82e-01 | 
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 31 | 8.89e-01 | 0.95200 | 0.06590 | -4.64e-02 | -0.046700 | 6.55e-01 | 6.53e-01 | 
| Selenocysteine synthesis | 68 | 7.68e-01 | 0.90600 | 0.06580 | -4.31e-02 | -0.049800 | 5.40e-01 | 4.79e-01 | 
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 21 | 7.92e-01 | 0.91600 | 0.06530 | 6.19e-03 | 0.065000 | 9.61e-01 | 6.06e-01 | 
| Formation of the beta-catenin:TCF transactivating complex | 22 | 7.98e-01 | 0.91600 | 0.06460 | 6.41e-02 | 0.008180 | 6.03e-01 | 9.47e-01 | 
| RHOF GTPase cycle | 22 | 6.63e-01 | 0.84800 | 0.06440 | -2.50e-02 | 0.059300 | 8.40e-01 | 6.30e-01 | 
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 15 | 9.47e-01 | 0.97300 | 0.06390 | 4.19e-02 | 0.048200 | 7.79e-01 | 7.47e-01 | 
| MAP2K and MAPK activation | 22 | 8.97e-01 | 0.95200 | 0.06380 | 5.60e-02 | 0.030700 | 6.50e-01 | 8.03e-01 | 
| Signaling by high-kinase activity BRAF mutants | 22 | 8.97e-01 | 0.95200 | 0.06380 | 5.60e-02 | 0.030700 | 6.50e-01 | 8.03e-01 | 
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 23 | 8.54e-01 | 0.94100 | 0.06370 | 2.07e-02 | 0.060200 | 8.63e-01 | 6.17e-01 | 
| Signaling by ERBB2 TMD/JMD mutants | 10 | 8.13e-01 | 0.91900 | 0.06360 | -4.74e-02 | 0.042400 | 7.95e-01 | 8.16e-01 | 
| RHO GTPase cycle | 269 | 3.76e-01 | 0.71100 | 0.06360 | 4.01e-02 | 0.049400 | 2.62e-01 | 1.67e-01 | 
| Cargo trafficking to the periciliary membrane | 37 | 4.81e-01 | 0.74200 | 0.06350 | 5.36e-02 | -0.034000 | 5.73e-01 | 7.20e-01 | 
| Global Genome Nucleotide Excision Repair (GG-NER) | 75 | 6.24e-01 | 0.82400 | 0.06350 | -2.30e-02 | -0.059200 | 7.32e-01 | 3.76e-01 | 
| Interleukin-17 signaling | 49 | 7.81e-01 | 0.91200 | 0.06350 | -5.62e-02 | -0.029500 | 4.97e-01 | 7.22e-01 | 
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 14 | 8.95e-01 | 0.95200 | 0.06300 | 1.53e-02 | 0.061100 | 9.21e-01 | 6.92e-01 | 
| Cargo concentration in the ER | 18 | 9.26e-01 | 0.96900 | 0.06290 | -3.36e-02 | -0.053100 | 8.05e-01 | 6.97e-01 | 
| Diseases associated with glycosylation precursor biosynthesis | 15 | 8.88e-01 | 0.95200 | 0.06280 | -1.53e-02 | -0.061000 | 9.18e-01 | 6.83e-01 | 
| Nucleotide Excision Repair | 98 | 2.78e-01 | 0.62100 | 0.06280 | 5.05e-03 | -0.062600 | 9.31e-01 | 2.86e-01 | 
| Gene expression (Transcription) | 941 | 5.35e-02 | 0.36100 | 0.06230 | -4.60e-02 | -0.042000 | 2.01e-02 | 3.40e-02 | 
| Glyoxylate metabolism and glycine degradation | 19 | 9.31e-01 | 0.97300 | 0.06200 | -5.00e-02 | -0.036700 | 7.06e-01 | 7.82e-01 | 
| Glycerophospholipid biosynthesis | 66 | 6.24e-01 | 0.82400 | 0.06190 | 5.95e-02 | 0.017100 | 4.04e-01 | 8.11e-01 | 
| Amyloid fiber formation | 25 | 9.17e-01 | 0.96500 | 0.06090 | -4.76e-02 | -0.038000 | 6.81e-01 | 7.42e-01 | 
| Fcgamma receptor (FCGR) dependent phagocytosis | 59 | 7.35e-01 | 0.89100 | 0.05950 | -2.31e-02 | -0.054800 | 7.59e-01 | 4.67e-01 | 
| Activated NOTCH1 Transmits Signal to the Nucleus | 19 | 8.20e-01 | 0.92100 | 0.05940 | -5.94e-02 | -0.000407 | 6.54e-01 | 9.98e-01 | 
| Diseases of mitotic cell cycle | 30 | 8.05e-01 | 0.91600 | 0.05920 | 5.77e-02 | 0.013300 | 5.85e-01 | 8.99e-01 | 
| Hemostasis | 279 | 3.64e-01 | 0.70600 | 0.05910 | 4.97e-02 | 0.032100 | 1.57e-01 | 3.61e-01 | 
| Signaling by NOTCH3 | 30 | 6.14e-01 | 0.82100 | 0.05890 | 5.26e-02 | -0.026400 | 6.18e-01 | 8.02e-01 | 
| PIWI-interacting RNA (piRNA) biogenesis | 15 | 7.70e-01 | 0.90600 | 0.05880 | 4.68e-02 | -0.035600 | 7.54e-01 | 8.11e-01 | 
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 75 | 7.81e-01 | 0.91200 | 0.05860 | -3.50e-02 | -0.047000 | 6.01e-01 | 4.83e-01 | 
| SUMOylation | 132 | 6.73e-01 | 0.85100 | 0.05840 | -4.37e-02 | -0.038700 | 3.88e-01 | 4.44e-01 | 
| Postmitotic nuclear pore complex (NPC) reformation | 25 | 7.81e-01 | 0.91200 | 0.05780 | -5.78e-02 | -0.000477 | 6.17e-01 | 9.97e-01 | 
| RHO GTPases activate PAKs | 13 | 8.75e-01 | 0.94900 | 0.05770 | 1.23e-03 | -0.057700 | 9.94e-01 | 7.19e-01 | 
| Response to elevated platelet cytosolic Ca2+ | 49 | 6.52e-01 | 0.84200 | 0.05750 | 5.73e-02 | 0.004710 | 4.89e-01 | 9.55e-01 | 
| TNFR1-induced proapoptotic signaling | 12 | 8.29e-01 | 0.92300 | 0.05730 | 2.70e-02 | -0.050600 | 8.71e-01 | 7.62e-01 | 
| Branched-chain amino acid catabolism | 20 | 7.41e-01 | 0.89100 | 0.05700 | 2.39e-02 | -0.051800 | 8.53e-01 | 6.89e-01 | 
| Nephrin family interactions | 12 | 8.99e-01 | 0.95200 | 0.05700 | 3.78e-03 | 0.056900 | 9.82e-01 | 7.33e-01 | 
| Signaling by ERBB2 in Cancer | 13 | 8.93e-01 | 0.95200 | 0.05640 | -5.63e-02 | -0.003550 | 7.25e-01 | 9.82e-01 | 
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 12 | 9.52e-01 | 0.97300 | 0.05590 | -2.50e-02 | -0.050000 | 8.81e-01 | 7.64e-01 | 
| Chaperonin-mediated protein folding | 51 | 5.18e-01 | 0.77400 | 0.05570 | -5.33e-02 | 0.016100 | 5.11e-01 | 8.42e-01 | 
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 55 | 6.22e-01 | 0.82400 | 0.05550 | -5.54e-02 | -0.002380 | 4.78e-01 | 9.76e-01 | 
| Signaling by Interleukins | 248 | 4.71e-01 | 0.73800 | 0.05460 | -4.55e-02 | -0.030200 | 2.21e-01 | 4.16e-01 | 
| Budding and maturation of HIV virion | 22 | 9.07e-01 | 0.95800 | 0.05460 | 5.03e-02 | 0.021100 | 6.83e-01 | 8.64e-01 | 
| Beta-catenin independent WNT signaling | 97 | 4.51e-01 | 0.73200 | 0.05450 | 5.44e-02 | 0.002670 | 3.56e-01 | 9.64e-01 | 
| Platelet activation, signaling and aggregation | 120 | 1.70e-01 | 0.51200 | 0.05430 | 4.28e-02 | -0.033400 | 4.19e-01 | 5.29e-01 | 
| DAP12 signaling | 17 | 9.01e-01 | 0.95300 | 0.05430 | -5.29e-02 | -0.012100 | 7.06e-01 | 9.31e-01 | 
| Transcriptional regulation of granulopoiesis | 23 | 7.53e-01 | 0.89700 | 0.05420 | -1.63e-02 | 0.051700 | 8.93e-01 | 6.68e-01 | 
| Negative regulators of DDX58/IFIH1 signaling | 32 | 6.93e-01 | 0.86700 | 0.05410 | -5.27e-02 | 0.012100 | 6.06e-01 | 9.06e-01 | 
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 46 | 5.75e-01 | 0.79500 | 0.05360 | 1.59e-02 | -0.051200 | 8.53e-01 | 5.48e-01 | 
| Phospholipid metabolism | 123 | 5.51e-01 | 0.78700 | 0.05340 | 5.06e-02 | 0.017000 | 3.34e-01 | 7.45e-01 | 
| Epigenetic regulation of gene expression | 73 | 8.28e-01 | 0.92300 | 0.05230 | 4.15e-02 | 0.031900 | 5.41e-01 | 6.38e-01 | 
| SUMOylation of transcription factors | 13 | 8.82e-01 | 0.94900 | 0.05220 | -6.90e-03 | 0.051800 | 9.66e-01 | 7.47e-01 | 
| RNA Polymerase II Transcription | 835 | 1.65e-01 | 0.51200 | 0.05180 | -3.60e-02 | -0.037200 | 8.50e-02 | 7.47e-02 | 
| Cytosolic sensors of pathogen-associated DNA | 52 | 7.33e-01 | 0.89100 | 0.05130 | -5.05e-02 | -0.008830 | 5.29e-01 | 9.12e-01 | 
| Negative epigenetic regulation of rRNA expression | 43 | 8.97e-01 | 0.95200 | 0.05120 | 4.10e-02 | 0.030600 | 6.42e-01 | 7.29e-01 | 
| Post-chaperonin tubulin folding pathway | 12 | 8.78e-01 | 0.94900 | 0.05110 | -4.89e-02 | 0.014700 | 7.69e-01 | 9.30e-01 | 
| Transcriptional Regulation by MECP2 | 27 | 7.14e-01 | 0.88100 | 0.05100 | -4.45e-02 | 0.024900 | 6.89e-01 | 8.23e-01 | 
| Phase II - Conjugation of compounds | 41 | 7.96e-01 | 0.91600 | 0.05100 | 1.05e-02 | 0.049900 | 9.08e-01 | 5.81e-01 | 
| Metabolism of amino acids and derivatives | 214 | 6.19e-01 | 0.82400 | 0.05100 | -3.70e-02 | -0.035100 | 3.54e-01 | 3.79e-01 | 
| Asymmetric localization of PCP proteins | 49 | 8.77e-01 | 0.94900 | 0.05080 | -2.83e-02 | -0.042200 | 7.32e-01 | 6.10e-01 | 
| Transcriptional regulation of white adipocyte differentiation | 55 | 8.58e-01 | 0.94100 | 0.05030 | 4.28e-02 | 0.026400 | 5.84e-01 | 7.35e-01 | 
| Endosomal Sorting Complex Required For Transport (ESCRT) | 25 | 7.33e-01 | 0.89100 | 0.04930 | 3.62e-02 | -0.033500 | 7.54e-01 | 7.72e-01 | 
| Transcriptional Regulation by VENTX | 24 | 7.80e-01 | 0.91200 | 0.04900 | 4.63e-02 | -0.016000 | 6.95e-01 | 8.92e-01 | 
| Platelet degranulation | 45 | 8.66e-01 | 0.94300 | 0.04830 | 4.38e-02 | 0.020400 | 6.11e-01 | 8.13e-01 | 
| Transcriptional activation of mitochondrial biogenesis | 39 | 8.29e-01 | 0.92300 | 0.04820 | -4.70e-02 | -0.010600 | 6.12e-01 | 9.09e-01 | 
| Diseases of signal transduction by growth factor receptors and second messengers | 284 | 5.68e-01 | 0.79000 | 0.04750 | -3.07e-02 | -0.036300 | 3.77e-01 | 2.97e-01 | 
| FCERI mediated Ca+2 mobilization | 22 | 9.54e-01 | 0.97300 | 0.04750 | 2.89e-02 | 0.037600 | 8.14e-01 | 7.60e-01 | 
| Disease | 1022 | 1.44e-01 | 0.49200 | 0.04740 | -2.92e-02 | -0.037300 | 1.26e-01 | 5.03e-02 | 
| RAB GEFs exchange GTP for GDP on RABs | 52 | 7.41e-01 | 0.89100 | 0.04730 | -4.60e-03 | -0.047100 | 9.54e-01 | 5.58e-01 | 
| Translation of Structural Proteins | 27 | 8.97e-01 | 0.95200 | 0.04720 | -1.39e-02 | -0.045200 | 9.01e-01 | 6.85e-01 | 
| Interleukin-12 signaling | 35 | 8.03e-01 | 0.91600 | 0.04720 | -1.92e-03 | -0.047100 | 9.84e-01 | 6.30e-01 | 
| Signal Transduction | 1254 | 1.18e-01 | 0.46600 | 0.04710 | 3.24e-02 | 0.034100 | 6.33e-02 | 5.04e-02 | 
| Nuclear Receptor transcription pathway | 26 | 9.49e-01 | 0.97300 | 0.04690 | -3.01e-02 | -0.036000 | 7.91e-01 | 7.51e-01 | 
| Diseases of metabolism | 120 | 7.50e-01 | 0.89700 | 0.04660 | 3.98e-02 | 0.024200 | 4.53e-01 | 6.48e-01 | 
| Antigen processing: Ubiquitination & Proteasome degradation | 224 | 5.49e-01 | 0.78600 | 0.04650 | 2.15e-02 | 0.041300 | 5.82e-01 | 2.90e-01 | 
| Signaling by ERBB2 ECD mutants | 10 | 9.76e-01 | 0.98300 | 0.04650 | 2.39e-02 | 0.039900 | 8.96e-01 | 8.27e-01 | 
| PCP/CE pathway | 68 | 5.38e-01 | 0.77600 | 0.04640 | 1.44e-02 | -0.044200 | 8.38e-01 | 5.30e-01 | 
| Signaling by NOTCH | 127 | 2.75e-01 | 0.61800 | 0.04600 | 3.97e-02 | -0.023300 | 4.41e-01 | 6.52e-01 | 
| Metabolism of proteins | 1162 | 1.29e-01 | 0.49100 | 0.04570 | -3.64e-02 | -0.027600 | 4.36e-02 | 1.27e-01 | 
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 25 | 9.46e-01 | 0.97300 | 0.04560 | -2.47e-02 | -0.038300 | 8.31e-01 | 7.40e-01 | 
| TCF dependent signaling in response to WNT | 112 | 8.17e-01 | 0.92100 | 0.04530 | 3.35e-02 | 0.030400 | 5.41e-01 | 5.79e-01 | 
| Semaphorin interactions | 34 | 7.11e-01 | 0.87900 | 0.04430 | -3.22e-02 | 0.030500 | 7.45e-01 | 7.59e-01 | 
| Protein folding | 57 | 6.31e-01 | 0.82800 | 0.04400 | -4.20e-02 | 0.013000 | 5.84e-01 | 8.65e-01 | 
| Autophagy | 93 | 8.34e-01 | 0.92600 | 0.04360 | 2.43e-02 | 0.036200 | 6.87e-01 | 5.47e-01 | 
| RNA Polymerase III Chain Elongation | 17 | 9.54e-01 | 0.97300 | 0.04310 | -1.66e-02 | -0.039700 | 9.05e-01 | 7.77e-01 | 
| Cyclin D associated events in G1 | 40 | 8.18e-01 | 0.92100 | 0.04260 | 2.24e-03 | 0.042500 | 9.80e-01 | 6.42e-01 | 
| G1 Phase | 40 | 8.18e-01 | 0.92100 | 0.04260 | 2.24e-03 | 0.042500 | 9.80e-01 | 6.42e-01 | 
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 19 | 9.46e-01 | 0.97300 | 0.04240 | 1.48e-02 | 0.039800 | 9.11e-01 | 7.64e-01 | 
| Activation of gene expression by SREBF (SREBP) | 34 | 8.26e-01 | 0.92300 | 0.04230 | 1.54e-03 | -0.042200 | 9.88e-01 | 6.70e-01 | 
| Cellular response to chemical stress | 137 | 3.43e-01 | 0.68300 | 0.04200 | -3.89e-02 | 0.015800 | 4.33e-01 | 7.50e-01 | 
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 31 | 9.38e-01 | 0.97300 | 0.04140 | -2.01e-02 | -0.036300 | 8.47e-01 | 7.27e-01 | 
| HIV Transcription Elongation | 31 | 9.38e-01 | 0.97300 | 0.04140 | -2.01e-02 | -0.036300 | 8.47e-01 | 7.27e-01 | 
| Tat-mediated elongation of the HIV-1 transcript | 31 | 9.38e-01 | 0.97300 | 0.04140 | -2.01e-02 | -0.036300 | 8.47e-01 | 7.27e-01 | 
| Transcriptional regulation by RUNX1 | 118 | 4.25e-01 | 0.71800 | 0.04110 | -1.37e-02 | 0.038800 | 7.98e-01 | 4.68e-01 | 
| Selective autophagy | 48 | 8.78e-01 | 0.94900 | 0.04070 | -3.82e-02 | -0.013900 | 6.47e-01 | 8.68e-01 | 
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 41 | 8.09e-01 | 0.91600 | 0.04050 | -1.50e-03 | 0.040500 | 9.87e-01 | 6.54e-01 | 
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 41 | 8.09e-01 | 0.91600 | 0.04050 | -1.50e-03 | 0.040500 | 9.87e-01 | 6.54e-01 | 
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 41 | 8.09e-01 | 0.91600 | 0.04050 | -1.50e-03 | 0.040500 | 9.87e-01 | 6.54e-01 | 
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 41 | 8.09e-01 | 0.91600 | 0.04050 | -1.50e-03 | 0.040500 | 9.87e-01 | 6.54e-01 | 
| Signaling by NOTCH1 in Cancer | 41 | 8.09e-01 | 0.91600 | 0.04050 | -1.50e-03 | 0.040500 | 9.87e-01 | 6.54e-01 | 
| ESR-mediated signaling | 110 | 6.93e-01 | 0.86700 | 0.04050 | -3.94e-02 | -0.009240 | 4.76e-01 | 8.67e-01 | 
| ATF4 activates genes in response to endoplasmic reticulum stress | 23 | 8.95e-01 | 0.95200 | 0.04000 | 2.17e-04 | -0.040000 | 9.99e-01 | 7.40e-01 | 
| Sphingolipid de novo biosynthesis | 18 | 9.76e-01 | 0.98300 | 0.03950 | -2.81e-02 | -0.027900 | 8.37e-01 | 8.38e-01 | 
| PI Metabolism | 58 | 8.60e-01 | 0.94100 | 0.03940 | 3.72e-02 | 0.013000 | 6.25e-01 | 8.65e-01 | 
| Keratan sulfate/keratin metabolism | 18 | 9.76e-01 | 0.98300 | 0.03910 | 2.65e-02 | 0.028800 | 8.46e-01 | 8.33e-01 | 
| Gastrin-CREB signalling pathway via PKC and MAPK | 11 | 9.27e-01 | 0.96900 | 0.03890 | 3.57e-02 | -0.015600 | 8.38e-01 | 9.29e-01 | 
| Cytoprotection by HMOX1 | 42 | 8.18e-01 | 0.92100 | 0.03880 | -1.80e-03 | 0.038700 | 9.84e-01 | 6.65e-01 | 
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 14 | 9.68e-01 | 0.98200 | 0.03870 | 1.41e-02 | 0.036000 | 9.27e-01 | 8.16e-01 | 
| CLEC7A (Dectin-1) induces NFAT activation | 11 | 9.52e-01 | 0.97300 | 0.03860 | 2.31e-04 | -0.038600 | 9.99e-01 | 8.24e-01 | 
| Signalling to ERKs | 25 | 9.51e-01 | 0.97300 | 0.03840 | 1.64e-02 | 0.034700 | 8.87e-01 | 7.64e-01 | 
| G alpha (12/13) signalling events | 33 | 9.25e-01 | 0.96900 | 0.03760 | 1.25e-02 | 0.035500 | 9.01e-01 | 7.25e-01 | 
| Adaptive Immune System | 439 | 3.69e-01 | 0.71100 | 0.03750 | 1.23e-02 | 0.035500 | 6.62e-01 | 2.08e-01 | 
| Glycosphingolipid metabolism | 25 | 8.56e-01 | 0.94100 | 0.03730 | -3.45e-02 | 0.014200 | 7.65e-01 | 9.02e-01 | 
| Formation of HIV elongation complex in the absence of HIV Tat | 32 | 9.60e-01 | 0.97800 | 0.03670 | -2.24e-02 | -0.029100 | 8.26e-01 | 7.76e-01 | 
| Macroautophagy | 85 | 7.38e-01 | 0.89100 | 0.03650 | 2.58e-03 | 0.036400 | 9.67e-01 | 5.62e-01 | 
| Neutrophil degranulation | 275 | 7.26e-01 | 0.89000 | 0.03650 | -2.38e-02 | -0.027600 | 5.00e-01 | 4.34e-01 | 
| Generic Transcription Pathway | 746 | 4.64e-01 | 0.73800 | 0.03560 | -2.50e-02 | -0.025400 | 2.56e-01 | 2.48e-01 | 
| Inflammasomes | 16 | 9.48e-01 | 0.97300 | 0.03510 | 3.50e-02 | 0.002510 | 8.09e-01 | 9.86e-01 | 
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 15 | 9.24e-01 | 0.96900 | 0.03510 | 3.33e-02 | -0.011000 | 8.24e-01 | 9.41e-01 | 
| Synthesis of PIPs at the Golgi membrane | 12 | 9.81e-01 | 0.98700 | 0.03500 | -3.13e-02 | -0.015600 | 8.51e-01 | 9.25e-01 | 
| Metabolism of porphyrins | 15 | 9.32e-01 | 0.97300 | 0.03480 | -3.41e-02 | 0.007090 | 8.19e-01 | 9.62e-01 | 
| Phosphorylation of the APC/C | 15 | 9.13e-01 | 0.96300 | 0.03480 | 2.11e-02 | -0.027600 | 8.87e-01 | 8.53e-01 | 
| RHOU GTPase cycle | 28 | 8.67e-01 | 0.94300 | 0.03440 | 3.24e-02 | -0.011500 | 7.67e-01 | 9.16e-01 | 
| Prolonged ERK activation events | 13 | 9.72e-01 | 0.98300 | 0.03410 | -3.28e-02 | -0.009450 | 8.38e-01 | 9.53e-01 | 
| NoRC negatively regulates rRNA expression | 41 | 9.53e-01 | 0.97300 | 0.03360 | 2.81e-02 | 0.018400 | 7.56e-01 | 8.39e-01 | 
| Signaling by Receptor Tyrosine Kinases | 279 | 5.66e-01 | 0.79000 | 0.03350 | 9.26e-03 | 0.032100 | 7.92e-01 | 3.59e-01 | 
| Signaling by Insulin receptor | 39 | 9.44e-01 | 0.97300 | 0.03280 | -2.98e-02 | -0.013700 | 7.48e-01 | 8.83e-01 | 
| Interferon gamma signaling | 50 | 8.51e-01 | 0.93900 | 0.03240 | -3.23e-02 | 0.000764 | 6.93e-01 | 9.93e-01 | 
| Sphingolipid metabolism | 43 | 8.94e-01 | 0.95200 | 0.03210 | -3.19e-02 | -0.003440 | 7.18e-01 | 9.69e-01 | 
| mRNA Capping | 25 | 8.81e-01 | 0.94900 | 0.03180 | 1.88e-02 | -0.025600 | 8.71e-01 | 8.25e-01 | 
| Signaling by Nuclear Receptors | 145 | 4.97e-01 | 0.75800 | 0.03170 | -1.63e-02 | 0.027200 | 7.36e-01 | 5.74e-01 | 
| Signaling by TGF-beta Receptor Complex | 68 | 7.40e-01 | 0.89100 | 0.03150 | -2.91e-02 | 0.012000 | 6.78e-01 | 8.65e-01 | 
| Constitutive Signaling by EGFRvIII | 10 | 9.74e-01 | 0.98300 | 0.03120 | 1.93e-03 | 0.031200 | 9.92e-01 | 8.65e-01 | 
| Signaling by EGFRvIII in Cancer | 10 | 9.74e-01 | 0.98300 | 0.03120 | 1.93e-03 | 0.031200 | 9.92e-01 | 8.65e-01 | 
| TNFR2 non-canonical NF-kB pathway | 62 | 9.50e-01 | 0.97300 | 0.03070 | -2.26e-02 | -0.020800 | 7.58e-01 | 7.78e-01 | 
| Extra-nuclear estrogen signaling | 47 | 9.23e-01 | 0.96800 | 0.02980 | 2.88e-02 | 0.007780 | 7.33e-01 | 9.27e-01 | 
| SHC1 events in ERBB2 signaling | 11 | 9.65e-01 | 0.98100 | 0.02940 | -2.89e-02 | 0.005430 | 8.68e-01 | 9.75e-01 | 
| Glutathione conjugation | 18 | 9.45e-01 | 0.97300 | 0.02940 | 2.90e-02 | -0.004340 | 8.31e-01 | 9.75e-01 | 
| RAF/MAP kinase cascade | 147 | 6.78e-01 | 0.85300 | 0.02930 | 2.92e-02 | -0.000900 | 5.42e-01 | 9.85e-01 | 
| Signalling to RAS | 12 | 9.69e-01 | 0.98200 | 0.02880 | -2.87e-02 | 0.001090 | 8.63e-01 | 9.95e-01 | 
| Activation of BAD and translocation to mitochondria | 14 | 9.47e-01 | 0.97300 | 0.02840 | -2.50e-02 | 0.013500 | 8.71e-01 | 9.30e-01 | 
| RNA Polymerase III Transcription Termination | 20 | 9.87e-01 | 0.99000 | 0.02770 | -1.97e-02 | -0.019500 | 8.79e-01 | 8.80e-01 | 
| Negative regulation of MAPK pathway | 35 | 9.68e-01 | 0.98200 | 0.02770 | 2.42e-02 | 0.013400 | 8.04e-01 | 8.91e-01 | 
| Selenoamino acid metabolism | 76 | 8.97e-01 | 0.95200 | 0.02720 | -7.00e-03 | -0.026300 | 9.16e-01 | 6.92e-01 | 
| RHOA GTPase cycle | 83 | 8.58e-01 | 0.94100 | 0.02700 | -2.68e-02 | -0.002780 | 6.73e-01 | 9.65e-01 | 
| FCGR3A-mediated IL10 synthesis | 19 | 9.37e-01 | 0.97300 | 0.02660 | 1.34e-02 | -0.022900 | 9.19e-01 | 8.63e-01 | 
| Nervous system development | 285 | 8.44e-01 | 0.93600 | 0.02510 | -2.02e-02 | -0.014900 | 5.60e-01 | 6.68e-01 | 
| Formation of the Early Elongation Complex | 25 | 9.84e-01 | 0.98800 | 0.02500 | 1.37e-02 | 0.020900 | 9.06e-01 | 8.57e-01 | 
| Formation of the HIV-1 Early Elongation Complex | 25 | 9.84e-01 | 0.98800 | 0.02500 | 1.37e-02 | 0.020900 | 9.06e-01 | 8.57e-01 | 
| Axon guidance | 275 | 8.64e-01 | 0.94200 | 0.02470 | -1.63e-02 | -0.018500 | 6.44e-01 | 6.00e-01 | 
| Mitochondrial biogenesis | 52 | 8.58e-01 | 0.94100 | 0.02450 | 2.06e-02 | -0.013300 | 7.98e-01 | 8.68e-01 | 
| Synthesis of PC | 21 | 9.65e-01 | 0.98100 | 0.02440 | 2.44e-02 | 0.000723 | 8.46e-01 | 9.95e-01 | 
| Signaling by MET | 37 | 9.70e-01 | 0.98200 | 0.02370 | -2.19e-02 | -0.009180 | 8.18e-01 | 9.23e-01 | 
| Innate Immune System | 563 | 6.16e-01 | 0.82200 | 0.02350 | -2.21e-02 | -0.007920 | 3.78e-01 | 7.52e-01 | 
| Glycogen storage diseases | 10 | 9.89e-01 | 0.99100 | 0.02350 | 5.68e-03 | 0.022800 | 9.75e-01 | 9.01e-01 | 
| Leishmania infection | 103 | 9.53e-01 | 0.97300 | 0.02300 | 1.53e-02 | 0.017200 | 7.89e-01 | 7.64e-01 | 
| Signaling by Rho GTPases | 407 | 5.41e-01 | 0.77800 | 0.02230 | 8.74e-04 | -0.022300 | 9.76e-01 | 4.46e-01 | 
| Factors involved in megakaryocyte development and platelet production | 82 | 9.51e-01 | 0.97300 | 0.02190 | -1.95e-02 | -0.009940 | 7.61e-01 | 8.77e-01 | 
| Post-translational modification: synthesis of GPI-anchored proteins | 29 | 9.36e-01 | 0.97300 | 0.02180 | 1.88e-02 | -0.011000 | 8.61e-01 | 9.19e-01 | 
| MHC class II antigen presentation | 66 | 9.15e-01 | 0.96300 | 0.02140 | -2.14e-02 | -0.000212 | 7.64e-01 | 9.98e-01 | 
| Metabolism of carbohydrates | 171 | 9.22e-01 | 0.96800 | 0.02040 | -1.03e-02 | -0.017600 | 8.18e-01 | 6.92e-01 | 
| EPH-Ephrin signaling | 53 | 9.36e-01 | 0.97300 | 0.01950 | 1.28e-03 | -0.019500 | 9.87e-01 | 8.06e-01 | 
| NRAGE signals death through JNK | 24 | 9.73e-01 | 0.98300 | 0.01890 | 1.88e-02 | -0.000925 | 8.73e-01 | 9.94e-01 | 
| Immune System | 1056 | 5.01e-01 | 0.76000 | 0.01850 | 3.89e-03 | 0.018100 | 8.36e-01 | 3.35e-01 | 
| Post-translational protein modification | 855 | 7.89e-01 | 0.91600 | 0.01840 | -1.22e-02 | -0.013800 | 5.55e-01 | 5.05e-01 | 
| Signaling by Rho GTPases, Miro GTPases and RHOBTB3 | 419 | 6.35e-01 | 0.83000 | 0.01660 | 4.40e-03 | -0.016000 | 8.79e-01 | 5.78e-01 | 
| Keratan sulfate biosynthesis | 14 | 9.91e-01 | 0.99200 | 0.01660 | 2.46e-03 | 0.016400 | 9.87e-01 | 9.15e-01 | 
| Ub-specific processing proteases | 128 | 9.48e-01 | 0.97300 | 0.01650 | 1.54e-02 | 0.006030 | 7.64e-01 | 9.06e-01 | 
| Developmental Biology | 429 | 8.91e-01 | 0.95200 | 0.01620 | -8.75e-03 | -0.013600 | 7.59e-01 | 6.32e-01 | 
| MAPK1/MAPK3 signaling | 152 | 8.23e-01 | 0.92200 | 0.01600 | 1.17e-02 | -0.010800 | 8.04e-01 | 8.19e-01 | 
| MAPK family signaling cascades | 176 | 8.98e-01 | 0.95200 | 0.01400 | 6.51e-04 | -0.013900 | 9.88e-01 | 7.51e-01 | 
| FLT3 Signaling | 27 | 9.92e-01 | 0.99200 | 0.01340 | -1.27e-02 | -0.004310 | 9.09e-01 | 9.69e-01 | 
| Deubiquitination | 189 | 8.85e-01 | 0.95100 | 0.01220 | 1.14e-02 | -0.004420 | 7.89e-01 | 9.17e-01 | 
| Class I MHC mediated antigen processing & presentation | 265 | 8.88e-01 | 0.95200 | 0.01220 | -3.00e-04 | 0.012200 | 9.93e-01 | 7.35e-01 | 
| Interleukin-12 family signaling | 41 | 9.88e-01 | 0.99100 | 0.00975 | 5.48e-05 | -0.009750 | 1.00e+00 | 9.14e-01 | 
| Metabolism | 1153 | 6.72e-01 | 0.85100 | 0.00955 | 3.03e-03 | -0.009060 | 8.67e-01 | 6.17e-01 |