| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:25119167-25119402 | Rare:31 | ||||
| chr15:25128542-25128619 | Rare:19 | ||||
| chr15:25397781-25397884 | Rare:22 | ||||
| chr15:25542205-25542369 | Rare:22 | ||||
| chr15:28176290-28176408 | Rare:31 | ||||
| chr15:28191052-28191191 | Rare:39 | ||||
| chr15:28238270-28238558 | Common:3; Rare:58 | ||||
| chr15:28684150-28684237 | Rare:8 | ||||
| chr15:28684251-28684551 | Common:4; Rare:30 | ||||
| chr15:29268263-29268387 | Common:1; Rare:38 | ||||
| chr15:29268401-29268548 | Common:4; Rare:29 | ||||
| chr15:29268577-29268642 | Rare:12 | ||||
| chr15:29268651-29268977 | Common:3; Rare:97; Clinvar (pathogenic):1 | ||||
| chr15:29268994-29269227 | Common:1; Rare:86; Clinvar (pathogenic):1 | ||||
| chr15:29674661-29675023 | Common:2; Rare:105 |