| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:102238684-102239014 | Common:7; Rare:137; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr8:102412692-102412977 | Common:3; Rare:70 | ||||
| chr8:102864153-102864445 | Common:2; Rare:116 | ||||
| chr8:103298724-103298911 | Common:1; Rare:45 | ||||
| chr8:103414785-103414962 | Rare:73 | ||||
| chr8:103414992-103415469 | Common:6; Rare:240 | ||||
| chr8:106657563-106657933 | Common:5; Rare:104 | ||||
| chr8:108248659-108248871 | Rare:87 | ||||
| chr8:108443440-108443673 | Common:4; Rare:106 | ||||
| chr8:109334018-109334447 | Common:1; Rare:132 | ||||
| chr8:109362352-109362519 | Common:1; Rare:30 | ||||
| chr8:109540398-109540423 | Rare:5 | ||||
| chr8:109540481-109540642 | Common:1; Rare:41 | ||||
| chr8:116852641-116852923 | Common:1; Rare:71; Clinvar (benign):1 | ||||
| chr8:116874611-116874935 | Common:6; Rare:136; Clinvar (benign):1 |