| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95317239-95317372 | Common:4; Rare:42 | ||||
| chr9:95317683-95317882 | Common:1; Rare:61; Clinvar:1 | ||||
| chr9:95505860-95506216 | Common:2; Rare:124 | ||||
| chr9:95875425-95875731 | Common:1; Rare:109 | ||||
| chr9:96778054-96778137 | Rare:26 | ||||
| chr9:97039056-97039260 | Rare:73 | ||||
| chr9:97633269-97633547 | Common:3; Rare:83 | ||||
| chr9:97633561-97633906 | Common:4; Rare:107 | ||||
| chr9:97697278-97697517 | Common:2; Rare:120; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922471-97922600 | Common:3; Rare:61 | ||||
| chr9:97983108-97983602 | Common:2; Rare:184 | ||||
| chr9:97984518-97984573 | Rare:25 | ||||
| chr9:98056409-98056785 | Common:5; Rare:114 | ||||
| chr9:99221906-99222356 | Common:2; Rare:175; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99906589-99906717 | Rare:56 |