| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:91040768-91041010 | Common:2; Rare:83 | ||||
| chr8:91069966-91070437 | Common:1; Rare:162 | ||||
| chr8:94553431-94553749 | Common:3; Rare:115 | ||||
| chr8:94949364-94949567 | Common:2; Rare:59 | ||||
| chr8:95024969-95025194 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr8:95268727-95268842 | Common:7; Rare:26 | ||||
| chr8:96235503-96235652 | Common:1; Rare:78; Clinvar (benign):2 | ||||
| chr8:96261566-96261981 | Common:6; Rare:137 | ||||
| chr8:97644647-97644881 | Common:1; Rare:79 | ||||
| chr8:97868987-97869115 | Rare:18 | ||||
| chr8:98045338-98045666 | Common:3; Rare:98 | ||||
| chr8:98117144-98117325 | Common:2; Rare:61 | ||||
| chr8:99013000-99013332 | Rare:66 | ||||
| chr8:100150575-100150709 | Rare:40 | ||||
| chr8:100309868-100310347 | Common:1; Rare:178 |