| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:110579769-110580040 | Common:2; Rare:73 | ||||
| chr9:110580056-110580088 | Rare:2 | ||||
| chr9:111038181-111038356 | Common:2; Rare:53 | ||||
| chr9:111038918-111039149 | Common:2; Rare:37 | ||||
| chr9:111661290-111661644 | Common:3; Rare:83 | ||||
| chr9:112379838-112380163 | Common:3; Rare:130 | ||||
| chr9:113056674-113056824 | Rare:56 | ||||
| chr9:113221230-113221597 | Common:1; Rare:118 | ||||
| chr9:113275381-113275734 | Common:5; Rare:114; Clinvar (pathogenic):1 | ||||
| chr9:113410281-113410729 | Common:3; Rare:135 | ||||
| chr9:114387967-114388104 | Common:1; Rare:47 | ||||
| chr9:116687235-116687361 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120533048-120533222 | Rare:37 | ||||
| chr9:120793200-120793534 | Common:1; Rare:116 | ||||
| chr9:120842905-120843089 | Common:1; Rare:65 |