| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97674779-97674988 | Rare:57 | ||||
| chr9:98045378-98045605 | Rare:40 | ||||
| chr9:100004418-100004622 | Rare:41 | ||||
| chr9:104787927-104788214 | Common:2; Rare:70; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:105065034-105065242 | Common:3; Rare:31 | ||||
| chr9:107637722-107637968 | Rare:50 | ||||
| chr9:110130426-110130516 | Rare:13 | ||||
| chr9:111662386-111662521 | Rare:19 | ||||
| chr9:111897860-111898106 | Common:3; Rare:42 | ||||
| chr9:112862304-112862445 | Rare:35 | ||||
| chr9:113173487-113173721 | Rare:54 | ||||
| chr9:113176614-113176759 | Common:1; Rare:30 | ||||
| chr9:114385460-114385740 | Common:4; Rare:56 | ||||
| chr9:114385746-114385885 | Common:1; Rare:29 | ||||
| chr9:114386552-114386652 | Rare:17 |