| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128998933-128999211 | Common:3; Rare:66; Clinvar (benign):1 | ||||
| chr9:129028090-129028217 | Common:1; Rare:35 | ||||
| chr9:129098270-129098575 | Rare:85 | ||||
| chr9:129110619-129111029 | Common:5; Rare:126 | ||||
| chr9:129111308-129111593 | Common:2; Rare:77 | ||||
| chr9:129139948-129140134 | Rare:36 | ||||
| chr9:129835112-129835496 | Common:4; Rare:148 | ||||
| chr9:130053860-130054031 | Common:1; Rare:66 | ||||
| chr9:130579456-130579686 | Common:6; Rare:98 | ||||
| chr9:130713442-130713676 | Common:2; Rare:51 | ||||
| chr9:131125287-131125649 | Common:3; Rare:139 | ||||
| chr9:131473316-131473546 | Common:4; Rare:40 | ||||
| chr9:131531120-131531342 | Common:9; Rare:97 | ||||
| chr9:132354926-132355246 | Common:4; Rare:106 | ||||
| chr9:132669920-132670046 | Common:1; Rare:60 |