| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35914513-35914563 | Rare:6 | ||||
| chr9:35914578-35914782 | Common:1; Rare:42 | ||||
| chr9:36145003-36145067 | Rare:4 | ||||
| chr9:36219926-36220191 | Common:1; Rare:54; Clinvar:6; Clinvar (pathogenic):2 | ||||
| chr9:36222940-36223100 | Rare:36; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr9:36234082-36234236 | Rare:32; Clinvar (benign):1 | ||||
| chr9:36274667-36274691 | Rare:2 | ||||
| chr9:37079764-37080033 | Common:4; Rare:80 | ||||
| chr9:37430343-37430593 | Rare:68; Clinvar (pathogenic):1 | ||||
| chr9:39809271-39809509 | Common:4; Rare:17 | ||||
| chr9:39809851-39809890 | Common:1; Rare:1 | ||||
| chr9:40106586-40106906 | Common:3; Rare:28 | ||||
| chr9:40584127-40584480 | Rare:4 | ||||
| chr9:40991948-40992495 | Common:8; Rare:39 | ||||
| chr9:40992605-40992666 | Rare:2 |