| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:71844408-71844612 | Common:2; Rare:50 | ||||
| chr8:72075569-72075648 | Common:1; Rare:15 | ||||
| chr8:73291569-73291908 | Rare:100 | ||||
| chr8:73292810-73292937 | Common:1; Rare:44 | ||||
| chr8:73294427-73294618 | Common:1; Rare:72 | ||||
| chr8:73295546-73295576 | Rare:7 | ||||
| chr8:73295805-73295923 | Common:2; Rare:32 | ||||
| chr8:73296907-73297186 | Common:1; Rare:69 | ||||
| chr8:73878809-73879009 | Common:3; Rare:97 | ||||
| chr8:73971913-73971957 | Rare:18 | ||||
| chr8:73972072-73972512 | Common:2; Rare:125 | ||||
| chr8:73975704-73975933 | Common:2; Rare:32 | ||||
| chr8:73976034-73976405 | Common:7; Rare:141; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:73991136-73991429 | Common:2; Rare:50 | ||||
| chr8:73991723-73991889 | Rare:25 |