Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73569032-73569292 | Rare:58 | ||||
chr14:73592052-73592163 | Common:2; Rare:39 | ||||
chr14:73644893-73645037 | Common:2; Rare:40; Clinvar:2 | ||||
chr14:73787121-73787379 | Common:2; Rare:88 | ||||
chr14:73851738-73851989 | Common:4; Rare:86 | ||||
chr14:73886768-73886876 | Common:1; Rare:36 | ||||
chr14:73950033-73950351 | Common:6; Rare:142; Clinvar (benign):5 | ||||
chr14:74019263-74019436 | Common:1; Rare:68 | ||||
chr14:74493246-74493822 | Common:4; Rare:192; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713070-74713207 | Rare:71 | ||||
chr14:74881651-74881998 | Common:1; Rare:134 | ||||
chr14:75002741-75002972 | Common:1; Rare:72; Clinvar:2 | ||||
chr14:75069455-75069689 | Common:2; Rare:61 | ||||
chr14:75126985-75127104 | Rare:39 | ||||
chr14:75278928-75279132 | Rare:66 |