| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129141813-129142050 | Common:4; Rare:62 | ||||
| chr9:129835185-129835481 | Common:2; Rare:121 | ||||
| chr9:130043053-130043336 | Common:2; Rare:95 | ||||
| chr9:130053804-130053965 | Common:1; Rare:59 | ||||
| chr9:130579456-130579754 | Common:6; Rare:113 | ||||
| chr9:130693615-130693800 | Rare:62 | ||||
| chr9:131096170-131096590 | Common:6; Rare:111 | ||||
| chr9:131125375-131125667 | Common:3; Rare:135 | ||||
| chr9:131502844-131502999 | Rare:61; Clinvar:3 | ||||
| chr9:132669960-132670045 | Common:1; Rare:41 | ||||
| chr9:133030442-133030742 | Common:4; Rare:82 | ||||
| chr9:133347966-133348386 | Common:4; Rare:159 | ||||
| chr9:133356426-133356614 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375947-133376340 | Common:3; Rare:141 | ||||
| chr9:133417939-133418296 | Common:4; Rare:86 |