| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97633357-97633825 | Common:6; Rare:146 | ||||
| chr9:97922513-97922580 | Common:1; Rare:31 | ||||
| chr9:99221927-99222349 | Common:2; Rare:157; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99906597-99906684 | Rare:43 | ||||
| chr9:100098978-100099314 | Common:2; Rare:93; Clinvar:2 | ||||
| chr9:100352919-100353071 | Rare:44 | ||||
| chr9:101398589-101398887 | Common:1; Rare:97 | ||||
| chr9:101487050-101487140 | Rare:29 | ||||
| chr9:101533711-101533871 | Rare:49 | ||||
| chr9:104093985-104094312 | Common:3; Rare:77 | ||||
| chr9:104094477-104094603 | Common:2; Rare:39 | ||||
| chr9:111599393-111599477 | Common:1; Rare:20 | ||||
| chr9:111661484-111661640 | Common:2; Rare:41 | ||||
| chr9:112379800-112380138 | Common:3; Rare:135 | ||||
| chr9:113056684-113056859 | Rare:59 |