| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44536657-44537401 | Common:3; Rare:243 | ||||
| chr15:44663556-44663846 | Rare:144; Clinvar:11; Clinvar (benign):6 | ||||
| chr15:44711341-44711611 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44711989 | Rare:26 | ||||
| chr15:44728848-44729205 | Common:1; Rare:76 | ||||
| chr15:45023007-45023267 | Common:3; Rare:71 | ||||
| chr15:45200496-45200656 | Common:1; Rare:44 | ||||
| chr15:45201099-45201143 | Common:1; Rare:23 | ||||
| chr15:45587103-45587470 | Common:1; Rare:89; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:45587703-45587815 | Common:1; Rare:27 | ||||
| chr15:45634929-45635084 | Rare:44 | ||||
| chr15:48330881-48331167 | Common:3; Rare:73 | ||||
| chr15:48331353-48331476 | Rare:42 | ||||
| chr15:48331893-48332359 | Common:6; Rare:153; Clinvar:1 | ||||
| chr15:48810959-48811358 | Common:4; Rare:101; Clinvar:4; Clinvar (benign):4 |