| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:101205094-101205689 | Common:5; Rare:174 | ||||
| chr8:101790908-101791132 | Rare:36 | ||||
| chr8:102238653-102238839 | Common:4; Rare:87; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr8:102238842-102239034 | Common:5; Rare:71; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:102239039-102239576 | Common:5; Rare:134 | ||||
| chr8:102412689-102412987 | Common:3; Rare:73 | ||||
| chr8:102655611-102655836 | Common:1; Rare:87 | ||||
| chr8:102864378-102864556 | Common:2; Rare:69 | ||||
| chr8:103020973-103021173 | Rare:64 | ||||
| chr8:103298689-103298988 | Common:2; Rare:73 | ||||
| chr8:103299278-103299411 | Common:2; Rare:28 | ||||
| chr8:103371388-103371806 | Common:1; Rare:164; Clinvar (pathogenic):1 | ||||
| chr8:103372203-103372556 | Common:1; Rare:64 | ||||
| chr8:103414658-103414742 | Common:5; Rare:30 | ||||
| chr8:103414766-103415516 | Common:6; Rare:355 |