Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:61762214-61762488 | Common:4; Rare:119 | ||||
chr14:63204238-63204455 | Rare:47 | ||||
chr14:63543342-63543613 | Common:3; Rare:76 | ||||
chr14:63641802-63642081 | Common:4; Rare:88 | ||||
chr14:63852887-63853071 | Common:1; Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
chr14:64212544-64212951 | Common:1; Rare:89; Clinvar (benign):1 | ||||
chr14:64294178-64294335 | Rare:40 | ||||
chr14:64294369-64294512 | Common:2; Rare:36 | ||||
chr14:64388095-64388404 | Common:2; Rare:127 | ||||
chr14:64503614-64503887 | Common:2; Rare:104 | ||||
chr14:64504572-64504837 | Rare:80 | ||||
chr14:64505228-64505347 | Rare:28 | ||||
chr14:64540506-64540753 | Common:1; Rare:63 | ||||
chr14:64914274-64914511 | Common:1; Rare:93 | ||||
chr14:64987097-64987262 | Rare:64 |