| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128881902-128882206 | Common:2; Rare:100 | ||||
| chr9:128947558-128947749 | Common:2; Rare:94; Clinvar:5; Clinvar (benign):2 | ||||
| chr9:129080788-129081131 | Common:2; Rare:93 | ||||
| chr9:129110649-129110949 | Common:3; Rare:66 | ||||
| chr9:129141537-129141758 | Common:2; Rare:70 | ||||
| chr9:129835185-129835492 | Common:2; Rare:124 | ||||
| chr9:130043119-130043345 | Common:2; Rare:82 | ||||
| chr9:130053864-130053972 | Common:1; Rare:48 | ||||
| chr9:130693571-130693794 | Rare:73 | ||||
| chr9:131125401-131125637 | Common:2; Rare:107 | ||||
| chr9:131502853-131503012 | Rare:61; Clinvar:3 | ||||
| chr9:131531182-131531342 | Common:9; Rare:72 | ||||
| chr9:132354947-132355290 | Common:5; Rare:111 | ||||
| chr9:132669936-132670046 | Common:1; Rare:53 | ||||
| chr9:133030461-133030743 | Common:4; Rare:76 |