| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:95024888-95025192 | Common:2; Rare:112; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:96235514-96235744 | Common:1; Rare:110; Clinvar (benign):2 | ||||
| chr8:96261566-96261981 | Common:6; Rare:137 | ||||
| chr8:96645193-96645377 | Common:1; Rare:48 | ||||
| chr8:98045387-98045642 | Common:3; Rare:79 | ||||
| chr8:98117120-98117356 | Common:4; Rare:74 | ||||
| chr8:99013000-99013332 | Rare:66 | ||||
| chr8:100150531-100150701 | Rare:59 | ||||
| chr8:100309874-100310263 | Common:1; Rare:136 | ||||
| chr8:100950536-100950675 | Common:8; Rare:81 | ||||
| chr8:101205434-101205816 | Common:5; Rare:111 | ||||
| chr8:103298719-103298944 | Common:2; Rare:54 | ||||
| chr8:103371398-103371643 | Common:1; Rare:79 | ||||
| chr8:103414800-103414911 | Rare:38 | ||||
| chr8:103414993-103415512 | Common:6; Rare:255 |