| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132354926-132355268 | Common:4; Rare:112 | ||||
| chr9:132406792-132406893 | Common:1; Rare:37 | ||||
| chr9:132669648-132669699 | Rare:11 | ||||
| chr9:132669932-132670075 | Common:1; Rare:65 | ||||
| chr9:132878314-132878385 | Common:1; Rare:22 | ||||
| chr9:133030442-133030742 | Common:4; Rare:82 | ||||
| chr9:133030920-133031023 | Rare:36 | ||||
| chr9:133336110-133336275 | Common:1; Rare:74 | ||||
| chr9:133348039-133348313 | Common:3; Rare:118 | ||||
| chr9:133356436-133356636 | Common:1; Rare:96; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375965-133376450 | Common:5; Rare:183 | ||||
| chr9:133418022-133418333 | Common:4; Rare:67 | ||||
| chr9:134135283-134135424 | Common:2; Rare:26 | ||||
| chr9:135961158-135961535 | Common:6; Rare:138 | ||||
| chr9:136410383-136410686 | Common:6; Rare:132 |