Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:75985709-75985802 | Rare:45; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr14:77377037-77377421 | Common:3; Rare:114 | ||||
chr14:77457563-77457876 | Common:1; Rare:93 | ||||
chr14:77708000-77708119 | Rare:55 | ||||
chr14:81220861-81221054 | Common:1; Rare:93 | ||||
chr14:81221288-81221438 | Common:1; Rare:35 | ||||
chr14:85529908-85530172 | Common:2; Rare:55 | ||||
chr14:88824342-88824716 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
chr14:89349965-89350326 | Rare:71 | ||||
chr14:89954644-89954954 | Rare:97 | ||||
chr14:90396870-90397151 | Common:5; Rare:142 | ||||
chr14:91114002-91114086 | Rare:23 | ||||
chr14:91836421-91836711 | Common:12; Rare:52 | ||||
chr14:92040028-92040082 | Common:1; Rare:19; Clinvar (benign):1 | ||||
chr14:92121658-92121985 | Common:4; Rare:109 |