| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38557450-38557920 | Common:9; Rare:142 | ||||
| chr8:38734403-38734919 | Common:5; Rare:169 | ||||
| chr8:38741930-38742560 | Common:4; Rare:154 | ||||
| chr8:40054670-40055140 | Common:6; Rare:137 | ||||
| chr8:40174510-40175110 | Common:4; Rare:187 | ||||
| chr8:41649860-41650130 | Common:1; Rare:65 | ||||
| chr8:41818680-41819010 | Common:2; Rare:80 | ||||
| chr8:42412738-42413301 | Common:2; Rare:168 | ||||
| chr8:42567419-42568216 | Common:10; Rare:151 | ||||
| chr8:60652256-60652404 | Common:2; Rare:50 | ||||
| chr8:60780651-60781620 | Common:5; Rare:346; Clinvar:18; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr8:61683190-61683490 | Common:2; Rare:52 | ||||
| chr8:61760040-61760630 | Common:21; Rare:197 | ||||
| chr8:61767070-61767580 | Rare:177 | ||||
| chr8:66925449-66925636 | Rare:131 |