| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:63382081-63382134 | Common:1; Rare:5 | ||||
| chr15:63505006-63505367 | Common:3; Rare:89 | ||||
| chr15:63515073-63515189 | Rare:19 | ||||
| chr15:63833456-63833602 | Rare:38 | ||||
| chr15:63833707-63834139 | Common:15; Rare:149 | ||||
| chr15:63834343-63834483 | Rare:39 | ||||
| chr15:64046216-64046281 | Rare:18 | ||||
| chr15:64046389-64046607 | Common:5; Rare:58 | ||||
| chr15:64093193-64093363 | Rare:37 | ||||
| chr15:64093651-64094227 | Common:3; Rare:174 | ||||
| chr15:64094228-64094384 | Common:1; Rare:30 | ||||
| chr15:64095779-64096084 | Common:6; Rare:111 | ||||
| chr15:64096357-64096509 | Rare:26 | ||||
| chr15:64153766-64153921 | Rare:33 | ||||
| chr15:64162903-64163458 | Common:5; Rare:169; Clinvar:6; Clinvar (benign):5 |