| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128947573-128947749 | Common:2; Rare:82; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:129110653-129110960 | Common:4; Rare:70 | ||||
| chr9:129835214-129835481 | Common:2; Rare:109 | ||||
| chr9:130053809-130053978 | Common:1; Rare:66 | ||||
| chr9:130579436-130579659 | Common:4; Rare:78 | ||||
| chr9:131125431-131125637 | Common:1; Rare:96 | ||||
| chr9:131270533-131270773 | Common:3; Rare:52 | ||||
| chr9:131502891-131503030 | Rare:47; Clinvar:3 | ||||
| chr9:131531170-131531357 | Common:9; Rare:86 | ||||
| chr9:132354932-132355257 | Common:4; Rare:107 | ||||
| chr9:132669945-132670101 | Common:1; Rare:75 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133348039-133348268 | Common:2; Rare:93 | ||||
| chr9:133356458-133356608 | Common:1; Rare:70; Clinvar (benign):2 | ||||
| chr9:133375965-133376366 | Common:3; Rare:146 |