Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:74881820-74881951 | Rare:54 | ||||
chr14:75002613-75002947 | Common:1; Rare:94; Clinvar:2 | ||||
chr14:75127008-75127110 | Rare:29 | ||||
chr14:75660825-75661003 | Rare:45 | ||||
chr14:75661189-75661299 | Common:2; Rare:28 | ||||
chr14:77377086-77377410 | Common:1; Rare:86 | ||||
chr14:77457563-77457869 | Common:1; Rare:92 | ||||
chr14:77708000-77708164 | Common:2; Rare:91 | ||||
chr14:81220861-81221046 | Common:1; Rare:91 | ||||
chr14:81221269-81221317 | Rare:8 | ||||
chr14:89954661-89954924 | Rare:78 | ||||
chr14:92040013-92040170 | Common:3; Rare:48; Clinvar:3; Clinvar (benign):2 | ||||
chr14:92121658-92122005 | Common:4; Rare:120 | ||||
chr14:93184878-93185008 | Rare:40 | ||||
chr14:93206985-93207294 | Common:2; Rare:152 |