| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:24912756-24912782 | Rare:1 | ||||
| chr8:24912978-24913255 | Common:2; Rare:45 | ||||
| chr8:24913625-24913773 | Rare:46 | ||||
| chr8:24914769-24915169 | Common:1; Rare:93; Clinvar:1 | ||||
| chr8:24955518-24956221 | Common:1; Rare:229; Clinvar:15; Clinvar (benign):10; Clinvar (pathogenic):4 | ||||
| chr8:24956406-24956450 | Rare:16; Clinvar:1 | ||||
| chr8:24956523-24956755 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:24956791-24956874 | Rare:18 | ||||
| chr8:25458306-25458621 | Common:2; Rare:83 | ||||
| chr8:26291396-26291812 | Common:3; Rare:142 | ||||
| chr8:26382902-26383133 | Common:3; Rare:98 | ||||
| chr8:26383250-26383429 | Rare:59 | ||||
| chr8:26512902-26513016 | Common:1; Rare:22 | ||||
| chr8:26513821-26514352 | Common:3; Rare:115 | ||||
| chr8:26578656-26578697 | Rare:8 |