| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97412007-97412174 | Common:3; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:97633292-97633884 | Common:6; Rare:184 | ||||
| chr9:97697304-97697520 | Common:1; Rare:102; Clinvar:5 | ||||
| chr9:97922480-97922600 | Common:2; Rare:56 | ||||
| chr9:98056496-98056810 | Common:2; Rare:106 | ||||
| chr9:98119175-98119322 | Common:1; Rare:37 | ||||
| chr9:98192623-98192841 | Common:5; Rare:61 | ||||
| chr9:99221940-99222365 | Common:2; Rare:161; Clinvar:3 | ||||
| chr9:99906570-99906717 | Rare:68 | ||||
| chr9:100098974-100099314 | Common:2; Rare:94; Clinvar:2 | ||||
| chr9:100352854-100353121 | Rare:100 | ||||
| chr9:101398556-101398895 | Common:1; Rare:124 | ||||
| chr9:101487097-101487178 | Common:1; Rare:18 | ||||
| chr9:104093985-104094371 | Common:5; Rare:98 | ||||
| chr9:104094486-104094595 | Common:2; Rare:33 |