| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:92095458-92095744 | Common:1; Rare:64 | ||||
| chr8:93700468-93700653 | Common:1; Rare:75 | ||||
| chr8:93740942-93741203 | Common:1; Rare:85 | ||||
| chr8:93916615-93917012 | Common:6; Rare:142; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:94436926-94437036 | Rare:26 | ||||
| chr8:94553445-94553749 | Common:3; Rare:107 | ||||
| chr8:94719779-94719945 | Common:1; Rare:48 | ||||
| chr8:94823148-94823312 | Common:1; Rare:49 | ||||
| chr8:95024956-95025144 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:96235510-96235652 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr8:96261586-96261943 | Common:5; Rare:111 | ||||
| chr8:98045499-98045642 | Common:2; Rare:47 | ||||
| chr8:98117123-98117325 | Common:2; Rare:69 | ||||
| chr8:99012998-99013368 | Rare:77; Clinvar:1 | ||||
| chr8:100150559-100150709 | Rare:45 |