| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92670024-92670351 | Common:1; Rare:98 | ||||
| chr9:93451455-93451702 | Common:3; Rare:69 | ||||
| chr9:93452314-93452388 | Rare:14 | ||||
| chr9:93452902-93452956 | Rare:13 | ||||
| chr9:93453546-93453696 | Rare:34 | ||||
| chr9:95507389-95507568 | Rare:46 | ||||
| chr9:95875449-95875699 | Common:1; Rare:83 | ||||
| chr9:95875961-95876037 | Common:4; Rare:37 | ||||
| chr9:96383597-96383777 | Common:3; Rare:53 | ||||
| chr9:96778046-96778134 | Rare:27 | ||||
| chr9:97501528-97501802 | Common:5; Rare:67 | ||||
| chr9:97633261-97633622 | Common:3; Rare:107 | ||||
| chr9:97633709-97633848 | Common:2; Rare:44 | ||||
| chr9:98943715-98943892 | Common:2; Rare:49 | ||||
| chr9:99221916-99222365 | Common:2; Rare:178; Clinvar:3; Clinvar (benign):2 |