| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128656635-128657038 | Common:2; Rare:128; Clinvar (pathogenic):1 | ||||
| chr9:128683406-128683513 | Common:1; Rare:17 | ||||
| chr9:128724070-128724443 | Common:1; Rare:126 | ||||
| chr9:128881912-128882186 | Common:1; Rare:92 | ||||
| chr9:128947523-128947716 | Common:1; Rare:87; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129110663-129110950 | Common:3; Rare:63 | ||||
| chr9:129139054-129139518 | Common:4; Rare:89 | ||||
| chr9:129835159-129835478 | Common:3; Rare:126 | ||||
| chr9:130053854-130053933 | Common:1; Rare:24 | ||||
| chr9:131125446-131125640 | Common:1; Rare:90 | ||||
| chr9:131502862-131503016 | Rare:56; Clinvar:3 | ||||
| chr9:132878282-132878408 | Common:1; Rare:47 | ||||
| chr9:133030447-133030776 | Common:4; Rare:94 | ||||
| chr9:133347984-133348249 | Common:3; Rare:88 | ||||
| chr9:133356417-133356599 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |