| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:22838356-22838717 | Common:3; Rare:129 | ||||
| chr15:23039543-23039719 | Common:1; Rare:69 | ||||
| chr15:30903747-30903936 | Common:1; Rare:51 | ||||
| chr15:34101843-34102083 | Common:1; Rare:48 | ||||
| chr15:34588447-34588567 | Rare:35 | ||||
| chr15:34988228-34988354 | Rare:53 | ||||
| chr15:36579496-36579731 | Common:3; Rare:67 | ||||
| chr15:39580864-39581097 | Common:1; Rare:61 | ||||
| chr15:39933883-39934187 | Common:4; Rare:93 | ||||
| chr15:40039092-40039329 | Rare:99 | ||||
| chr15:40340901-40341100 | Common:2; Rare:60 | ||||
| chr15:40405601-40405839 | Common:2; Rare:73; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr15:40755220-40755424 | Common:2; Rare:66 | ||||
| chr15:40807442-40807723 | Common:3; Rare:90 | ||||
| chr15:40844322-40844692 | Rare:132 |