| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45587093-45587265 | Rare:32 | ||||
| chr15:45587307-45587470 | Rare:49; Clinvar:6 | ||||
| chr15:45587703-45587785 | Rare:19 | ||||
| chr15:45634872-45635107 | Common:1; Rare:66 | ||||
| chr15:48178111-48178435 | Common:1; Rare:100 | ||||
| chr15:48331367-48331465 | Rare:32 | ||||
| chr15:48645663-48645893 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr15:48877981-48878590 | Common:1; Rare:228 | ||||
| chr15:49046327-49046658 | Common:2; Rare:115 | ||||
| chr15:49155538-49155842 | Common:2; Rare:100 | ||||
| chr15:49423099-49423425 | Common:1; Rare:54 | ||||
| chr15:49620752-49621122 | Common:6; Rare:137 | ||||
| chr15:50113289-50113385 | Rare:20 | ||||
| chr15:50354704-50354998 | Rare:85 | ||||
| chr15:50355074-50355514 | Common:3; Rare:177 |