| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128689529-128689650 | Rare:48 | ||||
| chr9:128724086-128724453 | Common:2; Rare:120 | ||||
| chr9:128881924-128882192 | Common:1; Rare:91 | ||||
| chr9:128947520-128947725 | Common:1; Rare:91; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129835143-129835490 | Common:3; Rare:138 | ||||
| chr9:130053846-130053989 | Common:1; Rare:60 | ||||
| chr9:130579431-130579700 | Common:7; Rare:107 | ||||
| chr9:132354912-132355288 | Common:5; Rare:125 | ||||
| chr9:132878279-132878400 | Common:1; Rare:46 | ||||
| chr9:133030447-133030771 | Common:4; Rare:92 | ||||
| chr9:133347980-133348268 | Common:3; Rare:104 | ||||
| chr9:133356284-133356607 | Common:5; Rare:149; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr9:133375925-133376366 | Common:3; Rare:152 | ||||
| chr9:133417953-133418293 | Common:4; Rare:80 | ||||
| chr9:136118831-136119041 | Common:3; Rare:89 |