| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:23084232-23084423 | Common:6; Rare:42 | ||||
| chr8:23457597-23457835 | Common:4; Rare:86 | ||||
| chr8:23528693-23529053 | Rare:117 | ||||
| chr8:23541474-23541762 | Common:3; Rare:55 | ||||
| chr8:24914869-24914974 | Rare:31 | ||||
| chr8:24955942-24956209 | Rare:97; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr8:24956608-24956702 | Common:2; Rare:23 | ||||
| chr8:25458221-25458618 | Common:2; Rare:114 | ||||
| chr8:26382750-26383176 | Common:3; Rare:153 | ||||
| chr8:26383512-26383671 | Common:1; Rare:33 | ||||
| chr8:26513865-26514205 | Common:1; Rare:75 | ||||
| chr8:27311236-27311683 | Common:10; Rare:143 | ||||
| chr8:27748566-27748757 | Common:1; Rare:48 | ||||
| chr8:27772559-27772709 | Common:4; Rare:53 | ||||
| chr8:27837701-27837919 | Common:2; Rare:60 |