| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:125579534-125579698 | Common:1; Rare:30 | ||||
| chr8:125642005-125642147 | Rare:30 | ||||
| chr8:125951136-125951230 | Rare:11 | ||||
| chr8:127041721-127041981 | Common:3; Rare:50 | ||||
| chr8:127737630-127737774 | Common:1; Rare:43 | ||||
| chr8:127794339-127794600 | Rare:68 | ||||
| chr8:127876756-127877035 | Common:4; Rare:51 | ||||
| chr8:129077735-129077871 | Rare:22 | ||||
| chr8:129148520-129148714 | Common:3; Rare:44 | ||||
| chr8:132868290-132868775 | Common:3; Rare:85 | ||||
| chr8:132869311-132869862 | Common:2; Rare:147; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr8:132871200-132871846 | Common:6; Rare:152; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:132875083-132875712 | Common:9; Rare:101 | ||||
| chr8:132877365-132877643 | Common:2; Rare:43 | ||||
| chr8:132877707-132877835 | Common:2; Rare:18 |