| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72474258-72474642 | Rare:138 | ||||
| chr15:72475144-72475418 | Common:2; Rare:74 | ||||
| chr15:72686154-72686226 | Common:2; Rare:28; Clinvar:3; Clinvar (benign):2 | ||||
| chr15:72758442-72758499 | Common:1; Rare:8 | ||||
| chr15:72783481-72783793 | Common:1; Rare:118 | ||||
| chr15:73633127-73633594 | Common:2; Rare:179 | ||||
| chr15:73752108-73752360 | Rare:59 | ||||
| chr15:73926329-73926466 | Rare:37 | ||||
| chr15:73994587-73994778 | Rare:40 | ||||
| chr15:74461101-74461314 | Rare:66 | ||||
| chr15:74540954-74541276 | Common:4; Rare:111 | ||||
| chr15:74615594-74615884 | Common:4; Rare:95 | ||||
| chr15:74843075-74843291 | Common:2; Rare:72 | ||||
| chr15:74873200-74873456 | Common:5; Rare:76 | ||||
| chr15:74889707-74890085 | Rare:103; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |