| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:101204967-101205174 | Common:1; Rare:40 | ||||
| chr8:101205603-101206039 | Common:2; Rare:119 | ||||
| chr8:101790745-101791120 | Rare:60 | ||||
| chr8:102123663-102124030 | Common:2; Rare:89 | ||||
| chr8:102238738-102238966 | Common:3; Rare:94; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr8:102412666-102413058 | Common:3; Rare:102 | ||||
| chr8:102653734-102654168 | Common:4; Rare:149 | ||||
| chr8:102655720-102655867 | Common:1; Rare:51 | ||||
| chr8:102656136-102656288 | Rare:52 | ||||
| chr8:102864118-102864340 | Common:3; Rare:99 | ||||
| chr8:102864658-102864803 | Rare:39 | ||||
| chr8:103020836-103021155 | Common:1; Rare:87 | ||||
| chr8:103140750-103141305 | Common:13; Rare:351 | ||||
| chr8:103415090-103415492 | Common:6; Rare:204 | ||||
| chr8:103500789-103501191 | Common:7; Rare:226 |