| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:23404116-23404262 | Common:2; Rare:36 | ||||
| chr8:23457609-23457841 | Common:4; Rare:85 | ||||
| chr8:23528714-23529075 | Rare:113 | ||||
| chr8:24913071-24913187 | Common:1; Rare:16 | ||||
| chr8:24913660-24913766 | Rare:33 | ||||
| chr8:24914845-24915063 | Rare:52 | ||||
| chr8:24955922-24956193 | Rare:100; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr8:25458206-25458552 | Common:2; Rare:99 | ||||
| chr8:25458721-25459031 | Common:2; Rare:90 | ||||
| chr8:25459151-25459313 | Common:3; Rare:66 | ||||
| chr8:26291363-26291508 | Common:1; Rare:61 | ||||
| chr8:26382870-26383093 | Rare:86 | ||||
| chr8:26383304-26383461 | Rare:43 | ||||
| chr8:26513851-26514236 | Common:1; Rare:85 | ||||
| chr8:27258384-27258623 | Rare:34 |