| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:93134228-93134354 | Common:2; Rare:45 | ||||
| chr9:93452292-93452354 | Rare:9 | ||||
| chr9:93453534-93453687 | Rare:36 | ||||
| chr9:94259269-94259338 | Rare:21 | ||||
| chr9:94726562-94726734 | Rare:46 | ||||
| chr9:95317653-95317852 | Common:1; Rare:65; Clinvar:2 | ||||
| chr9:95505871-95506216 | Common:2; Rare:118 | ||||
| chr9:95516762-95517081 | Common:2; Rare:92; Clinvar (pathogenic):1 | ||||
| chr9:95875441-95875759 | Common:1; Rare:115 | ||||
| chr9:95875932-95876084 | Common:6; Rare:70; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96655294-96655376 | Rare:24 | ||||
| chr9:96778040-96778163 | Rare:37 | ||||
| chr9:97039132-97039419 | Common:1; Rare:109 | ||||
| chr9:97633251-97633872 | Common:6; Rare:191 | ||||
| chr9:97666649-97666804 | Common:1; Rare:26 |