| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130579446-130579665 | Common:3; Rare:78 | ||||
| chr9:130693588-130693794 | Rare:67 | ||||
| chr9:131096267-131096585 | Common:3; Rare:87 | ||||
| chr9:131125407-131125619 | Common:2; Rare:94 | ||||
| chr9:131502853-131503040 | Rare:71; Clinvar:3 | ||||
| chr9:131531182-131531350 | Common:9; Rare:76 | ||||
| chr9:132161091-132161238 | Rare:29 | ||||
| chr9:132354955-132355186 | Common:3; Rare:75 | ||||
| chr9:132669930-132670039 | Common:1; Rare:52 | ||||
| chr9:132878264-132878385 | Common:1; Rare:45 | ||||
| chr9:133030447-133030742 | Common:4; Rare:78 | ||||
| chr9:133336128-133336360 | Common:1; Rare:95 | ||||
| chr9:133348025-133348253 | Common:3; Rare:84 | ||||
| chr9:133356436-133356658 | Common:1; Rare:104; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133376024-133376340 | Common:1; Rare:116 |