| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:60512073-60512141 | Rare:20 | ||||
| chr15:60592462-60592733 | Common:1; Rare:72 | ||||
| chr15:60706318-60706437 | Rare:19 | ||||
| chr15:62060364-62060570 | Rare:80 | ||||
| chr15:62060756-62060785 | Common:1; Rare:1 | ||||
| chr15:62390435-62390632 | Common:1; Rare:95 | ||||
| chr15:63042464-63042938 | Common:6; Rare:147; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63043021-63043202 | Common:1; Rare:29 | ||||
| chr15:63048297-63048710 | Common:4; Rare:149; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63122502-63122659 | Common:4; Rare:63 | ||||
| chr15:63157413-63157782 | Common:6; Rare:136 | ||||
| chr15:63188929-63189048 | Common:1; Rare:31 | ||||
| chr15:63189393-63189667 | Common:2; Rare:92 | ||||
| chr15:63277261-63277698 | Common:4; Rare:98 | ||||
| chr15:63291452-63291570 | Common:1; Rare:16 |