| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:23528575-23528909 | Rare:84 | ||||
| chr8:26382971-26383123 | Common:2; Rare:70 | ||||
| chr8:26513870-26513999 | Rare:27 | ||||
| chr8:27311226-27311493 | Common:7; Rare:106 | ||||
| chr8:27490922-27491155 | Common:3; Rare:56 | ||||
| chr8:27614680-27614946 | Rare:87 | ||||
| chr8:27772555-27772767 | Common:6; Rare:68 | ||||
| chr8:27774422-27774580 | Common:2; Rare:33; Clinvar (benign):1 | ||||
| chr8:30095338-30095504 | Common:1; Rare:54 | ||||
| chr8:30156250-30156386 | Rare:36 | ||||
| chr8:30744093-30744257 | Common:3; Rare:64 | ||||
| chr8:33485022-33485224 | Common:2; Rare:70 | ||||
| chr8:37737567-37737854 | Rare:36 | ||||
| chr8:37762478-37762683 | Common:2; Rare:74 | ||||
| chr8:38030370-38030589 | Common:2; Rare:70 |