| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:107489767-107490101 | Common:4; Rare:148 | ||||
| chr9:108934074-108934493 | Common:7; Rare:169; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110048545-110048759 | Common:2; Rare:80 | ||||
| chr9:110579184-110579322 | Rare:44 | ||||
| chr9:110579330-110579372 | Rare:14 | ||||
| chr9:110579374-110579423 | Rare:17 | ||||
| chr9:110579547-110579724 | Common:1; Rare:48 | ||||
| chr9:110579784-110580103 | Common:2; Rare:74 | ||||
| chr9:111038178-111038357 | Common:2; Rare:55 | ||||
| chr9:111038673-111039010 | Common:6; Rare:79 | ||||
| chr9:111599624-111599867 | Common:1; Rare:69 | ||||
| chr9:111631137-111631304 | Rare:32 | ||||
| chr9:111661505-111661673 | Common:3; Rare:52 | ||||
| chr9:112379753-112380193 | Common:4; Rare:163 | ||||
| chr9:113056697-113056919 | Rare:69 |