| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45114073-45114267 | Common:2; Rare:36 | ||||
| chr15:45114311-45114412 | Rare:21 | ||||
| chr15:45114471-45114613 | Common:1; Rare:47 | ||||
| chr15:45114679-45114693 | Rare:4 | ||||
| chr15:45129821-45129944 | Rare:25 | ||||
| chr15:45129951-45130073 | Rare:24 | ||||
| chr15:45130424-45130510 | Rare:10 | ||||
| chr15:45150464-45150701 | Common:3; Rare:53 | ||||
| chr15:45201094-45201159 | Common:1; Rare:33 | ||||
| chr15:45378475-45378665 | Common:4; Rare:52; Clinvar:1; Clinvar (benign):4 | ||||
| chr15:45402211-45402354 | Common:2; Rare:39 | ||||
| chr15:45522346-45522672 | Rare:84 | ||||
| chr15:45587090-45587273 | Rare:33 | ||||
| chr15:45587281-45587635 | Common:1; Rare:117; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:45587703-45587831 | Common:1; Rare:30 |