Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:34462219-34462542 | Common:1; Rare:112 | ||||
chr14:34875302-34875383 | Rare:34 | ||||
chr14:34982372-34982634 | Common:1; Rare:105 | ||||
chr14:35046119-35046531 | Common:2; Rare:138 | ||||
chr14:35122244-35122756 | Common:2; Rare:146 | ||||
chr14:35292179-35292462 | Common:4; Rare:102 | ||||
chr14:35402755-35403143 | Common:4; Rare:112; Clinvar (benign):4 | ||||
chr14:36320544-36320783 | Common:4; Rare:84 | ||||
chr14:37197865-37198103 | Common:3; Rare:74 | ||||
chr14:39432420-39432618 | Common:6; Rare:66 | ||||
chr14:44961892-44962255 | Common:3; Rare:105 | ||||
chr14:49586334-49586776 | Common:1; Rare:238 | ||||
chr14:49598670-49598961 | Common:1; Rare:114 | ||||
chr14:49620573-49620837 | Common:2; Rare:109; Clinvar:3 | ||||
chr14:49892814-49893135 | Common:1; Rare:141 |