| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:94593775-94593904 | Rare:22 | ||||
| chr9:94726572-94726732 | Rare:43 | ||||
| chr9:95507405-95507436 | Rare:11 | ||||
| chr9:95875448-95875709 | Common:1; Rare:89 | ||||
| chr9:95875965-95876056 | Common:5; Rare:45 | ||||
| chr9:96778078-96778154 | Rare:21 | ||||
| chr9:97501528-97501802 | Common:5; Rare:67 | ||||
| chr9:97633282-97633872 | Common:6; Rare:187 | ||||
| chr9:97697206-97697392 | Common:1; Rare:111; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922463-97922574 | Common:3; Rare:58 | ||||
| chr9:98255600-98255915 | Common:3; Rare:98 | ||||
| chr9:98943802-98943951 | Common:3; Rare:52 | ||||
| chr9:99221906-99222358 | Common:2; Rare:176; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99821695-99822033 | Rare:93 | ||||
| chr9:99906563-99906717 | Rare:69 |