| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128771916-128772031 | Rare:22 | ||||
| chr9:128772450-128772487 | Rare:3 | ||||
| chr9:128947578-128947716 | Common:1; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129835214-129835464 | Common:2; Rare:105 | ||||
| chr9:130053854-130053935 | Common:1; Rare:26 | ||||
| chr9:131125416-131125637 | Common:2; Rare:102 | ||||
| chr9:132354955-132355244 | Common:4; Rare:96 | ||||
| chr9:133030447-133030742 | Common:4; Rare:78 | ||||
| chr9:133348087-133348258 | Common:1; Rare:72 | ||||
| chr9:133356458-133356628 | Common:1; Rare:80; Clinvar (benign):2 | ||||
| chr9:133376007-133376366 | Common:1; Rare:131 | ||||
| chr9:136410390-136410686 | Common:6; Rare:128 | ||||
| chr9:137188547-137188711 | Common:2; Rare:77 | ||||
| chr9:137551653-137551964 | Common:27; Rare:133 | ||||
| chr9:137618797-137619035 | Common:1; Rare:107 |