| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:93916637-93917019 | Common:4; Rare:137; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:94436656-94436966 | Rare:77 | ||||
| chr8:94436984-94437122 | Rare:29 | ||||
| chr8:94553444-94553739 | Common:3; Rare:104 | ||||
| chr8:94719772-94720011 | Common:1; Rare:76 | ||||
| chr8:94823148-94823350 | Common:2; Rare:71 | ||||
| chr8:94895688-94895822 | Common:1; Rare:37 | ||||
| chr8:94949360-94949553 | Common:1; Rare:57 | ||||
| chr8:95269198-95269339 | Common:6; Rare:53; Clinvar:1 | ||||
| chr8:96235510-96235652 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr8:96261574-96261965 | Common:5; Rare:131 | ||||
| chr8:96493636-96494330 | Common:4; Rare:217 | ||||
| chr8:97644647-97644851 | Common:1; Rare:70 | ||||
| chr8:98045348-98045666 | Common:3; Rare:96 | ||||
| chr8:98117114-98117345 | Common:4; Rare:78 |