| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92878010-92878214 | Common:2; Rare:58 | ||||
| chr9:93134228-93134352 | Common:2; Rare:45 | ||||
| chr9:93451462-93451702 | Common:3; Rare:69 | ||||
| chr9:93453546-93453687 | Rare:31 | ||||
| chr9:94259291-94259338 | Rare:15 | ||||
| chr9:95317655-95317852 | Common:1; Rare:64; Clinvar:2 | ||||
| chr9:95875449-95875703 | Common:1; Rare:84 | ||||
| chr9:95875961-95876037 | Common:4; Rare:37 | ||||
| chr9:97633271-97633399 | Rare:33 | ||||
| chr9:97633572-97633855 | Common:3; Rare:92 | ||||
| chr9:97922471-97922574 | Common:3; Rare:52 | ||||
| chr9:97983106-97983578 | Common:2; Rare:177 | ||||
| chr9:98056444-98056789 | Common:2; Rare:110 | ||||
| chr9:98192618-98192869 | Common:6; Rare:67 | ||||
| chr9:99221906-99222355 | Common:2; Rare:175; Clinvar:2; Clinvar (benign):2 |