| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128947607-128947735 | Common:1; Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129824098-129824278 | Common:3; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:129835210-129835472 | Common:2; Rare:108 | ||||
| chr9:130053854-130053978 | Common:1; Rare:52 | ||||
| chr9:130579461-130579677 | Common:6; Rare:89 | ||||
| chr9:131125435-131125661 | Common:1; Rare:109 | ||||
| chr9:131531182-131531326 | Common:4; Rare:66 | ||||
| chr9:132669939-132670039 | Common:1; Rare:49 | ||||
| chr9:132878308-132878402 | Common:1; Rare:34 | ||||
| chr9:133030447-133030742 | Common:4; Rare:78 | ||||
| chr9:133336110-133336309 | Common:1; Rare:89 | ||||
| chr9:133348080-133348276 | Common:1; Rare:87 | ||||
| chr9:133356443-133356616 | Common:1; Rare:81; Clinvar (benign):2 | ||||
| chr9:133375999-133376366 | Common:1; Rare:133 | ||||
| chr9:133479075-133479377 | Common:1; Rare:85 |