| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:22440980-22441301 | Common:5; Rare:79 | ||||
| chr8:22551586-22551971 | Common:1; Rare:89 | ||||
| chr8:22565219-22565292 | Rare:27 | ||||
| chr8:22604704-22605085 | Common:4; Rare:149 | ||||
| chr8:22614201-22614462 | Common:3; Rare:89 | ||||
| chr8:22669055-22669241 | Common:2; Rare:75 | ||||
| chr8:22999744-22999990 | Common:1; Rare:60 | ||||
| chr8:23068981-23069198 | Common:1; Rare:86 | ||||
| chr8:23164014-23164262 | Rare:47 | ||||
| chr8:23225070-23225233 | Common:1; Rare:38 | ||||
| chr8:23457613-23457824 | Common:3; Rare:75 | ||||
| chr8:24913540-24913776 | Rare:59 | ||||
| chr8:24955886-24956156 | Rare:108; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr8:26382912-26383213 | Common:3; Rare:133 | ||||
| chr8:26383224-26383419 | Rare:67 |