| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:69414198-69414453 | Rare:86 | ||||
| chr15:69452590-69452657 | Rare:16 | ||||
| chr15:69452737-69453020 | Common:5; Rare:117 | ||||
| chr15:70763394-70763840 | Common:2; Rare:140 | ||||
| chr15:70853957-70854293 | Rare:99 | ||||
| chr15:70892363-70892859 | Common:1; Rare:109 | ||||
| chr15:72118028-72118425 | Common:3; Rare:135 | ||||
| chr15:72231094-72231546 | Common:3; Rare:147 | ||||
| chr15:72375958-72376124 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474178-72474316 | Rare:50 | ||||
| chr15:72686135-72686236 | Common:2; Rare:38; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:73633259-73633602 | Common:2; Rare:128 | ||||
| chr15:73926265-73926482 | Rare:53 | ||||
| chr15:73994587-73994761 | Rare:34 | ||||
| chr15:74461086-74461416 | Rare:94 |