Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35046130-35046472 | Common:1; Rare:114 | ||||
chr14:35122250-35122574 | Common:1; Rare:93 | ||||
chr14:35292224-35292451 | Common:3; Rare:84 | ||||
chr14:35404637-35404875 | Common:2; Rare:88; Clinvar (benign):2 | ||||
chr14:35533925-35534164 | Common:3; Rare:92 | ||||
chr14:37197880-37198043 | Common:1; Rare:49 | ||||
chr14:39432420-39432625 | Common:6; Rare:69 | ||||
chr14:44961896-44962278 | Common:3; Rare:111 | ||||
chr14:49586347-49586720 | Common:1; Rare:195 | ||||
chr14:49620580-49620771 | Common:2; Rare:70 | ||||
chr14:49795908-49796165 | Rare:41 | ||||
chr14:50312201-50312325 | Rare:43 | ||||
chr14:50532518-50532674 | Common:2; Rare:46 | ||||
chr14:51095071-51095297 | Common:4; Rare:87 | ||||
chr14:51240210-51240287 | Rare:35 |