| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128724014-128724464 | Common:2; Rare:167 | ||||
| chr9:128947593-128947735 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129110667-129110949 | Common:3; Rare:63 | ||||
| chr9:129139897-129140114 | Rare:44 | ||||
| chr9:129835210-129835481 | Common:2; Rare:111 | ||||
| chr9:130053854-130053929 | Common:1; Rare:24 | ||||
| chr9:130579461-130579641 | Common:2; Rare:55 | ||||
| chr9:131125413-131125637 | Common:2; Rare:103 | ||||
| chr9:132669952-132670039 | Common:1; Rare:43 | ||||
| chr9:132878286-132878370 | Common:1; Rare:30 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133336141-133336351 | Common:1; Rare:83 | ||||
| chr9:133348043-133348253 | Common:2; Rare:79 | ||||
| chr9:133356457-133356599 | Common:1; Rare:65; Clinvar (benign):2 | ||||
| chr9:133375941-133376264 | Common:2; Rare:112 |