| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:32550821-32551187 | Common:1; Rare:145; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33511122-33511191 | Rare:24 | ||||
| chr9:33676782-33676821 | Common:1; Rare:10 | ||||
| chr9:33677003-33677452 | Common:13; Rare:150 | ||||
| chr9:34552608-34552683 | Rare:17 | ||||
| chr9:35603968-35604196 | Common:3; Rare:67 | ||||
| chr9:35657724-35657764 | Common:1; Rare:26; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:36499593-36499782 | Common:1; Rare:32 | ||||
| chr9:37027621-37027953 | Common:3; Rare:97 | ||||
| chr9:37079760-37080027 | Common:4; Rare:78 | ||||
| chr9:37465922-37466006 | Common:2; Rare:25 | ||||
| chr9:37466506-37466642 | Common:2; Rare:27 | ||||
| chr9:37923361-37923652 | Common:3; Rare:53 | ||||
| chr9:38375719-38375886 | Common:3; Rare:41 | ||||
| chr9:38421821-38422271 | Common:3; Rare:84 |