| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41416989-41417202 | Common:2; Rare:95 | ||||
| chr15:41972544-41972718 | Rare:45 | ||||
| chr15:42273050-42273272 | Common:1; Rare:96 | ||||
| chr15:42273400-42273627 | Rare:82 | ||||
| chr15:42495468-42495694 | Common:2; Rare:63 | ||||
| chr15:42548725-42548875 | Common:2; Rare:84 | ||||
| chr15:43330593-43330711 | Rare:42 | ||||
| chr15:43493101-43493350 | Common:1; Rare:76 | ||||
| chr15:43746287-43746428 | Common:1; Rare:50 | ||||
| chr15:44536863-44537206 | Common:1; Rare:123 | ||||
| chr15:44711346-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45129850-45130021 | Rare:38 | ||||
| chr15:45378532-45378707 | Common:3; Rare:42; Clinvar (benign):1 | ||||
| chr15:45587117-45587482 | Common:1; Rare:93; Clinvar:6; Clinvar (benign):2 | ||||
| chr15:45634883-45635084 | Rare:52 |