| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45634921-45635100 | Rare:51 | ||||
| chr15:45645701-45645955 | Common:1; Rare:49 | ||||
| chr15:48330893-48331123 | Common:2; Rare:50 | ||||
| chr15:48331383-48331465 | Rare:27 | ||||
| chr15:48645710-48645930 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr15:48877995-48878422 | Rare:162 | ||||
| chr15:49046267-49046613 | Common:2; Rare:125 | ||||
| chr15:49155528-49155933 | Common:4; Rare:125 | ||||
| chr15:49423111-49423266 | Common:1; Rare:32 | ||||
| chr15:49620752-49621121 | Common:6; Rare:136 | ||||
| chr15:50354703-50354998 | Rare:85 | ||||
| chr15:50355074-50355513 | Common:3; Rare:176 | ||||
| chr15:50424138-50424466 | Common:2; Rare:119 | ||||
| chr15:50686617-50686898 | Common:4; Rare:105 | ||||
| chr15:50765529-50765715 | Common:1; Rare:65 |