| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131531179-131531350 | Common:9; Rare:77 | ||||
| chr9:132406801-132406895 | Rare:33 | ||||
| chr9:132669930-132670039 | Common:1; Rare:52 | ||||
| chr9:132878272-132878381 | Common:1; Rare:40 | ||||
| chr9:133030471-133030742 | Common:4; Rare:69 | ||||
| chr9:133336128-133336351 | Common:1; Rare:91 | ||||
| chr9:133348039-133348314 | Common:3; Rare:118 | ||||
| chr9:133356449-133356614 | Common:1; Rare:78; Clinvar (benign):2 | ||||
| chr9:133376003-133376366 | Common:1; Rare:132 | ||||
| chr9:133418034-133418296 | Common:4; Rare:53 | ||||
| chr9:133479092-133479326 | Common:1; Rare:65 | ||||
| chr9:135499860-135499966 | Common:2; Rare:28 | ||||
| chr9:136410609-136410686 | Rare:40 | ||||
| chr9:137086706-137087006 | Common:1; Rare:111; Clinvar:1 | ||||
| chr9:137087038-137087125 | Common:1; Rare:39; Clinvar:1 |