| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132669939-132670051 | Common:1; Rare:53 | ||||
| chr9:132878278-132878414 | Common:1; Rare:53 | ||||
| chr9:132878754-132878945 | Rare:35 | ||||
| chr9:133030447-133030742 | Common:4; Rare:78 | ||||
| chr9:133336128-133336418 | Common:2; Rare:124 | ||||
| chr9:133348039-133348253 | Common:2; Rare:80 | ||||
| chr9:133356458-133356630 | Common:1; Rare:81; Clinvar (benign):2 | ||||
| chr9:133375999-133376370 | Common:1; Rare:133 | ||||
| chr9:133459904-133460021 | Rare:51 | ||||
| chr9:134641523-134641809 | Common:2; Rare:86; Clinvar (benign):1 | ||||
| chr9:136410417-136410668 | Common:6; Rare:109 | ||||
| chr9:136848635-136848789 | Rare:43 | ||||
| chr9:136849574-136849782 | Common:1; Rare:80 | ||||
| chr9:136944604-136944909 | Common:2; Rare:115 | ||||
| chr9:137086819-137087139 | Common:1; Rare:137; Clinvar:6; Clinvar (benign):1 |