| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94719761-94719955 | Common:1; Rare:53 | ||||
| chr8:95024945-95025109 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr8:96235510-96235661 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr8:96261574-96261967 | Common:5; Rare:131 | ||||
| chr8:98045387-98045645 | Common:3; Rare:80 | ||||
| chr8:98117055-98117379 | Common:4; Rare:109 | ||||
| chr8:99013000-99013332 | Rare:66 | ||||
| chr8:100150322-100150709 | Common:1; Rare:98 | ||||
| chr8:100309897-100310269 | Common:1; Rare:135 | ||||
| chr8:100950399-100950712 | Common:11; Rare:128 | ||||
| chr8:100953279-100953479 | Common:1; Rare:44 | ||||
| chr8:101205543-101205874 | Common:4; Rare:103 | ||||
| chr8:101492254-101492501 | Common:2; Rare:41 | ||||
| chr8:101492539-101492826 | Common:1; Rare:63; Clinvar (benign):2 | ||||
| chr8:102864119-102864461 | Common:4; Rare:136 |