| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33473841-33474144 | Common:4; Rare:94 | ||||
| chr9:33750577-33750700 | Rare:39 | ||||
| chr9:34048870-34049014 | Common:1; Rare:58 | ||||
| chr9:34049170-34049268 | Common:1; Rare:26 | ||||
| chr9:34049275-34049612 | Common:1; Rare:104 | ||||
| chr9:34126362-34126461 | Rare:39 | ||||
| chr9:34126574-34126850 | Common:1; Rare:84 | ||||
| chr9:34178928-34179063 | Common:1; Rare:35 | ||||
| chr9:34329166-34329656 | Common:1; Rare:149 | ||||
| chr9:34458539-34458875 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:34612071-34612230 | Common:8; Rare:57 | ||||
| chr9:34620447-34620597 | Common:1; Rare:44 | ||||
| chr9:34637676-34637953 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:34646535-34646733 | Common:1; Rare:61; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr9:34652010-34652217 | Rare:59 |