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. 2019 Oct 24;12:144. doi: 10.1186/s12920-019-0602-8

Table 4.

Top five diseases influenced by CHH differential methylation

Disease Molecules related to Disease FDR Molecules
Familial skeletal dysplasia ADAMTS2, DDR2, FAM20C, FDFT1, MYO18B, PDE4D, ROR2, TNFRSF11A 3.06E-07 8
Large intestine adenocarcinoma ADAMTS2, AGT, ATXN3L, BAIAP2L1, CCDC155, CCDC85C, CFAP299, CMIP, CNNM2, CTDP1, DDR2, DNAJB13, FAM20C, FDFT1, FPR3, GAS7, GCM1, GRID2, IL13, IL27, IQCE, ITPK1, KCNJ12, KRT38, MCEE, MYO18B, NAV2, NDUFA10, NPHP4, PCSK6, PDE4D, PGS1, PITPNC1, PLEKHF1, PLEKHM3, PRKCA, PTPRN2, RALGPS2, RASA3, RIMBP2, RIN2, ROR2, RPS19, SLC30A1, SLC6A12, SPATS2L, SPG7, SV2C, TDRD5, TMEM92, TNFRSF11A, ZFYVE28 2.34E-06 52
Hereditary connective tissue disorder ADAMTS2, AGT, CTDP1, DDR2, FAM20C, FDFT1, JDP2, MYO18B, PDE4D, RIN2, ROR2, TNFRSF11A 2.76E-06 12
Abdominal adenocarcinoma ADAMTS2, AGT, ATXN3L, BAIAP2L1, CCDC155, CCDC85C, CFAP299, CMIP, CNNM2, CPNE6, CTDP1, DDR2, DNAJB13, FAM20C, FDFT1, FPR3, GAS7, GCM1, GRID2, IL13, IL27, IQCE, ITPK1, KCNJ12, KRT38, MCEE, MYO18B, NAV2, NDUFA10, NPHP4, PCSK6, PDE4D, PGS1, PITPNC1, PLEKHF1, PLEKHM3, PRKCA, PTPRN2, RALGPS2, RASA3, RIMBP2, RIN2, ROR2, RPS19, SLC30A1, SLC6A12, SPATS2L, SPG7, SSR1, SV2C, TDRD5, TMEM92, TNFRSF11A, ZFYVE28 8.89E-05 54
Liver carcinoma ADAMTS2, AGT, CNNM2, CTDP1, DDR2, DNAJB13, FAM20C, FPR3, GAS7, GRID2, IL27, IQCE, JDP2, KCNJ12, MYO18B, NAV2, NDUFA10, NPHP4, PDE4D, PGS1, PITPNC1, PTPRN2, RALGPS2, RASA3, RIMBP2, RIN2, SLC30A1, SLC6A12, TDRD5, TNFRSF11A, ZFYVE28 2.32E-04 31