| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128371181-128371375 | Rare:65 | ||||
| chr9:128552398-128552593 | Rare:71; Clinvar:1 | ||||
| chr9:128656652-128656794 | Common:2; Rare:66; Clinvar (pathogenic):1 | ||||
| chr9:128724070-128724475 | Common:3; Rare:136 | ||||
| chr9:128947604-128947716 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129110693-129110955 | Common:3; Rare:57 | ||||
| chr9:129835228-129835475 | Common:2; Rare:97 | ||||
| chr9:130053854-130053915 | Common:1; Rare:18 | ||||
| chr9:130579456-130579641 | Common:2; Rare:56 | ||||
| chr9:130693619-130693783 | Rare:54 | ||||
| chr9:131531213-131531379 | Common:10; Rare:69 | ||||
| chr9:132878279-132878349 | Common:1; Rare:24 | ||||
| chr9:133348097-133348247 | Common:1; Rare:60 | ||||
| chr9:133356449-133356593 | Common:1; Rare:65; Clinvar (benign):2 | ||||
| chr9:133375995-133376340 | Common:2; Rare:126 |