Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35046139-35046559 | Common:1; Rare:144 | ||||
chr14:35121932-35122597 | Common:3; Rare:195 | ||||
chr14:35292224-35292469 | Common:3; Rare:91 | ||||
chr14:35404634-35404830 | Common:2; Rare:77; Clinvar (benign):2 | ||||
chr14:37197896-37198087 | Common:2; Rare:61 | ||||
chr14:38207839-38207961 | Rare:18 | ||||
chr14:39114156-39114356 | Common:2; Rare:73 | ||||
chr14:39170264-39170471 | Common:3; Rare:64 | ||||
chr14:39175029-39175272 | Common:3; Rare:84 | ||||
chr14:39432459-39432624 | Common:6; Rare:56 | ||||
chr14:41608179-41608341 | Rare:37 | ||||
chr14:44961892-44962272 | Common:3; Rare:110 | ||||
chr14:45083984-45084174 | Common:1; Rare:71 | ||||
chr14:45253078-45253299 | Rare:58 | ||||
chr14:49586342-49586772 | Common:1; Rare:229 |