| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:23272613-23272862 | Common:3; Rare:59 | ||||
| chr8:24514818-24514974 | Common:1; Rare:25 | ||||
| chr8:24524843-24524983 | Common:1; Rare:19 | ||||
| chr8:24955602-24955832 | Rare:66; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr8:25278437-25278605 | Rare:40 | ||||
| chr8:25365538-25365571 | Rare:5 | ||||
| chr8:25685695-25685875 | Common:1; Rare:35 | ||||
| chr8:25833429-25833553 | Common:2; Rare:15 | ||||
| chr8:25840127-25840245 | Rare:32 | ||||
| chr8:26206777-26206900 | Common:1; Rare:20 | ||||
| chr8:27012433-27012536 | Common:1; Rare:20 | ||||
| chr8:27592345-27592497 | Common:1; Rare:34 | ||||
| chr8:27592898-27593002 | Rare:28 | ||||
| chr8:27593342-27593463 | Rare:70 | ||||
| chr8:27608932-27609248 | Rare:71 |