| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44194408-44194559 | Rare:32 | ||||
| chr15:44288406-44288962 | Common:39; Rare:277 | ||||
| chr15:44427550-44427762 | Common:1; Rare:53 | ||||
| chr15:44536663-44536777 | Rare:23 | ||||
| chr15:44536859-44537430 | Common:3; Rare:203 | ||||
| chr15:44710767-44710859 | Common:1; Rare:15 | ||||
| chr15:44711342-44711613 | Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711898-44712015 | Rare:24 | ||||
| chr15:45587117-45587274 | Rare:28 | ||||
| chr15:45587287-45587618 | Common:1; Rare:112; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:48178082-48178417 | Common:1; Rare:102 | ||||
| chr15:48331126-48331465 | Common:5; Rare:117 | ||||
| chr15:48331854-48332251 | Common:7; Rare:118 | ||||
| chr15:48645636-48646145 | Common:3; Rare:157; Clinvar (benign):1 | ||||
| chr15:48878034-48878684 | Common:1; Rare:230 |