| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129110647-129111029 | Common:5; Rare:118 | ||||
| chr9:129835210-129835498 | Common:3; Rare:115 | ||||
| chr9:130053847-130053978 | Common:1; Rare:54 | ||||
| chr9:130451928-130452349 | Common:2; Rare:123; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr9:130579428-130579641 | Common:3; Rare:64 | ||||
| chr9:130713442-130713662 | Common:2; Rare:50 | ||||
| chr9:131125446-131125649 | Common:1; Rare:98 | ||||
| chr9:131502865-131503040 | Rare:62; Clinvar:3 | ||||
| chr9:131518173-131518489 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:132669930-132670046 | Common:1; Rare:55 | ||||
| chr9:132670170-132670500 | Rare:110 | ||||
| chr9:133030471-133030742 | Common:4; Rare:69 | ||||
| chr9:133275179-133275302 | Rare:25 | ||||
| chr9:133348039-133348253 | Common:2; Rare:80 | ||||
| chr9:133356452-133356618 | Common:1; Rare:79; Clinvar (benign):2 |