| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45378462-45378618 | Common:3; Rare:46; Clinvar:1; Clinvar (benign):5 | ||||
| chr15:45402190-45402360 | Common:2; Rare:50 | ||||
| chr15:45587099-45587273 | Rare:30 | ||||
| chr15:45587311-45587609 | Rare:104; Clinvar:5; Clinvar (benign):2 | ||||
| chr15:45587649-45587828 | Common:2; Rare:54 | ||||
| chr15:45634668-45634849 | Common:1; Rare:43 | ||||
| chr15:45634929-45635096 | Rare:50 | ||||
| chr15:48178128-48178217 | Common:1; Rare:39 | ||||
| chr15:48331350-48331476 | Rare:43 | ||||
| chr15:48645698-48645956 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr15:48878055-48878908 | Common:2; Rare:274 | ||||
| chr15:49046345-49046605 | Common:2; Rare:97 | ||||
| chr15:49155530-49155867 | Common:2; Rare:112 | ||||
| chr15:49170088-49170299 | Rare:44 | ||||
| chr15:49423111-49423398 | Common:1; Rare:47 |