| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:62060276-62060551 | Rare:103 | ||||
| chr15:62165281-62165384 | Rare:28 | ||||
| chr15:62390411-62390633 | Common:1; Rare:118 | ||||
| chr15:62758423-62758651 | Common:2; Rare:34 | ||||
| chr15:63042889-63042948 | Rare:16; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr15:63048268-63048706 | Common:5; Rare:164; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63157402-63157550 | Common:2; Rare:64 | ||||
| chr15:63189314-63189675 | Common:2; Rare:116 | ||||
| chr15:63277317-63277641 | Common:4; Rare:63 | ||||
| chr15:63504377-63504747 | Common:2; Rare:126 | ||||
| chr15:63553456-63553749 | Common:2; Rare:46 | ||||
| chr15:63588474-63588792 | Rare:57 | ||||
| chr15:63615890-63616265 | Common:4; Rare:80 | ||||
| chr15:63833873-63834038 | Common:1; Rare:63 | ||||
| chr15:64046306-64046612 | Common:14; Rare:97 |