| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128771839-128772067 | Common:2; Rare:70 | ||||
| chr9:128947545-128947725 | Common:1; Rare:82; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129110667-129110953 | Common:3; Rare:65 | ||||
| chr9:129835225-129835471 | Common:2; Rare:99 | ||||
| chr9:130053665-130053939 | Common:1; Rare:66 | ||||
| chr9:130579436-130579718 | Common:7; Rare:112 | ||||
| chr9:132669622-132669719 | Rare:26 | ||||
| chr9:132878282-132878408 | Common:1; Rare:47 | ||||
| chr9:133030447-133030755 | Common:4; Rare:85 | ||||
| chr9:133336088-133336244 | Common:1; Rare:81 | ||||
| chr9:133348006-133348276 | Common:3; Rare:105 | ||||
| chr9:133356417-133356607 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375925-133376334 | Common:3; Rare:141 | ||||
| chr9:133417953-133418309 | Common:4; Rare:82 | ||||
| chr9:134641552-134641845 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):1 |