Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35292175-35292478 | Common:5; Rare:110; Clinvar:1 | ||||
chr14:35404572-35404839 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
chr14:35826347-35826465 | Rare:32 | ||||
chr14:35826717-35826930 | Common:1; Rare:58 | ||||
chr14:36320584-36320783 | Common:3; Rare:61 | ||||
chr14:37197844-37198093 | Common:3; Rare:82 | ||||
chr14:39114156-39114356 | Common:2; Rare:73 | ||||
chr14:39267022-39267428 | Common:2; Rare:143 | ||||
chr14:39432407-39432650 | Common:6; Rare:84 | ||||
chr14:44961892-44962258 | Common:3; Rare:106 | ||||
chr14:45083943-45084174 | Common:1; Rare:92 | ||||
chr14:45253161-45253291 | Rare:31 | ||||
chr14:49586327-49586772 | Common:1; Rare:237; Clinvar (benign):1 | ||||
chr14:49620573-49620842 | Common:2; Rare:112; Clinvar:3 | ||||
chr14:49892934-49893143 | Rare:85 |