| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45587648-45587966 | Common:3; Rare:86 | ||||
| chr15:45587975-45588127 | Rare:30 | ||||
| chr15:45631427-45631619 | Rare:36 | ||||
| chr15:45634610-45635164 | Common:2; Rare:145 | ||||
| chr15:45645558-45645601 | Rare:4 | ||||
| chr15:45645680-45645908 | Common:1; Rare:41 | ||||
| chr15:48177870-48177913 | Rare:10 | ||||
| chr15:48178123-48178199 | Rare:31 | ||||
| chr15:48178214-48178426 | Rare:53 | ||||
| chr15:48330887-48331230 | Common:3; Rare:93 | ||||
| chr15:48331300-48331899 | Common:8; Rare:212 | ||||
| chr15:48332005-48332186 | Rare:49 | ||||
| chr15:48644626-48644843 | Rare:68; Clinvar:6; Clinvar (benign):8 | ||||
| chr15:48644850-48645024 | Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:48645027-48645114 | Rare:19 |