| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128656676-128656816 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
| chr9:128724090-128724464 | Common:2; Rare:123 | ||||
| chr9:128771860-128772005 | Rare:38 | ||||
| chr9:128787143-128787348 | Common:3; Rare:71 | ||||
| chr9:128881901-128882206 | Common:2; Rare:100 | ||||
| chr9:128921976-128922314 | Common:1; Rare:75 | ||||
| chr9:128947567-128947732 | Common:1; Rare:76; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129110625-129110949 | Common:3; Rare:72 | ||||
| chr9:129111087-129111360 | Common:3; Rare:74 | ||||
| chr9:129139903-129140132 | Rare:45 | ||||
| chr9:129626113-129626200 | Rare:33 | ||||
| chr9:129824093-129824293 | Common:3; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:129835210-129835484 | Common:2; Rare:111 | ||||
| chr9:130043090-130043296 | Common:2; Rare:63 | ||||
| chr9:130053854-130053939 | Common:1; Rare:28 |