| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:115118021-115118237 | Common:3; Rare:53 | ||||
| chr9:116687235-116687364 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120532545-120532728 | Rare:41 | ||||
| chr9:120533034-120533205 | Rare:34 | ||||
| chr9:120714452-120714689 | Common:2; Rare:73 | ||||
| chr9:120793231-120793543 | Common:2; Rare:114 | ||||
| chr9:120842905-120843274 | Common:1; Rare:117 | ||||
| chr9:120843324-120843412 | Rare:22 | ||||
| chr9:120868841-120869060 | Common:2; Rare:45 | ||||
| chr9:120877177-120877451 | Common:1; Rare:84 | ||||
| chr9:121074811-121074976 | Rare:81 | ||||
| chr9:121075104-121075164 | Rare:16 | ||||
| chr9:121201802-121202158 | Common:2; Rare:110 | ||||
| chr9:121268037-121268213 | Common:1; Rare:62 | ||||
| chr9:121299637-121299990 | Common:2; Rare:109; Clinvar:3 |