| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:88902254-88902307 | Common:1; Rare:11 | ||||
| chr15:88904323-88904642 | Common:1; Rare:47 | ||||
| chr15:88913114-88913470 | Common:4; Rare:97 | ||||
| chr15:89088114-89088556 | Common:5; Rare:102 | ||||
| chr15:89328696-89328959 | Common:1; Rare:84; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr15:89334778-89335041 | Common:1; Rare:92 | ||||
| chr15:89496804-89497102 | Rare:53 | ||||
| chr15:89575171-89575522 | Common:1; Rare:99 | ||||
| chr15:89690673-89690785 | Common:2; Rare:36 | ||||
| chr15:90233872-90234275 | Common:6; Rare:115 | ||||
| chr15:90265640-90265727 | Rare:40 | ||||
| chr15:90352127-90352323 | Common:3; Rare:50 | ||||
| chr15:90387909-90388396 | Common:6; Rare:190 | ||||
| chr15:90473683-90474129 | Common:2; Rare:132 | ||||
| chr15:90529839-90529970 | Common:2; Rare:53 |