| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132944546-132944955 | Common:1; Rare:140; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133163874-133164013 | Common:3; Rare:39 | ||||
| chr9:133348014-133348268 | Common:3; Rare:99 | ||||
| chr9:133356399-133356630 | Common:1; Rare:109; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:133375947-133376412 | Common:5; Rare:166 | ||||
| chr9:133417964-133418329 | Common:4; Rare:88 | ||||
| chr9:133459946-133460044 | Common:1; Rare:44 | ||||
| chr9:133534545-133534707 | Rare:48 | ||||
| chr9:133636089-133636396 | Rare:68 | ||||
| chr9:133738317-133738464 | Common:1; Rare:41 | ||||
| chr9:134067974-134068238 | Rare:71 | ||||
| chr9:134135303-134135430 | Common:2; Rare:21 | ||||
| chr9:136118812-136119005 | Common:4; Rare:85 | ||||
| chr9:136410603-136410697 | Common:1; Rare:51 |