| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67121160-67121300 | Common:3; Rare:23 | ||||
| chr15:67121223-67121373 | Common:2; Rare:28 | ||||
| chr15:67134134-67134560 | Common:9; Rare:121 | ||||
| chr15:67135190-67135470 | Common:2; Rare:54 | ||||
| chr15:67140066-67140975 | Common:12; Rare:225 | ||||
| chr15:67164720-67165080 | Common:2; Rare:86; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr15:67173450-67173730 | Common:1; Rare:48 | ||||
| chr15:67241291-67241515 | Rare:62 | ||||
| chr15:67542028-67542176 | Common:1; Rare:27 | ||||
| chr15:67680505-67680938 | Common:6; Rare:111 | ||||
| chr15:67839690-67840045 | Common:5; Rare:296 | ||||
| chr15:67840046-67840481 | Common:11; Rare:495 | ||||
| chr15:67840609-67841292 | Common:10; Rare:164 | ||||
| chr15:67841240-67841730 | Common:5; Rare:94 | ||||
| chr15:67851142-67851525 | Common:4; Rare:66 |