| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131125446-131125696 | Common:1; Rare:117 | ||||
| chr9:131502869-131503016 | Rare:52; Clinvar:3 | ||||
| chr9:131531182-131531326 | Common:4; Rare:66 | ||||
| chr9:132354929-132355339 | Common:5; Rare:134 | ||||
| chr9:132669930-132670061 | Common:1; Rare:59 | ||||
| chr9:132878308-132878403 | Common:1; Rare:34 | ||||
| chr9:132878823-132878985 | Rare:29 | ||||
| chr9:133030442-133030743 | Common:4; Rare:83 | ||||
| chr9:133129369-133129419 | Common:1; Rare:13 | ||||
| chr9:133275171-133275383 | Rare:45 | ||||
| chr9:133336128-133336330 | Common:1; Rare:82 | ||||
| chr9:133348039-133348309 | Common:3; Rare:117 | ||||
| chr9:133350723-133351064 | Common:2; Rare:140 | ||||
| chr9:133356443-133356614 | Common:1; Rare:80; Clinvar (benign):2 | ||||
| chr9:133375925-133376370 | Common:3; Rare:152 |