| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45634850-45635088 | Rare:62 | ||||
| chr15:47717149-47717519 | Common:1; Rare:77 | ||||
| chr15:47717985-47718245 | Common:1; Rare:58 | ||||
| chr15:47718427-47718744 | Common:1; Rare:68 | ||||
| chr15:48331367-48331453 | Rare:27 | ||||
| chr15:48645710-48645913 | Common:2; Rare:65; Clinvar (benign):1 | ||||
| chr15:48878034-48878394 | Rare:130 | ||||
| chr15:49155528-49155882 | Common:2; Rare:117 | ||||
| chr15:49620806-49621093 | Common:6; Rare:113 | ||||
| chr15:50182306-50182448 | Rare:39 | ||||
| chr15:50354680-50354972 | Common:1; Rare:92 | ||||
| chr15:50355116-50355545 | Common:3; Rare:185 | ||||
| chr15:50424308-50424466 | Common:1; Rare:69 | ||||
| chr15:50686713-50686999 | Common:6; Rare:111 | ||||
| chr15:50908582-50908769 | Common:2; Rare:79; Clinvar (benign):2 |