| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131502835-131503210 | Rare:119; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:131531170-131531350 | Common:9; Rare:82 | ||||
| chr9:132354922-132355212 | Common:3; Rare:95 | ||||
| chr9:132406774-132406944 | Common:1; Rare:56 | ||||
| chr9:132669648-132669867 | Rare:65 | ||||
| chr9:132669930-132670051 | Common:1; Rare:56 | ||||
| chr9:132878272-132878414 | Common:1; Rare:56 | ||||
| chr9:132944467-132944684 | Rare:79; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:133030454-133030744 | Common:4; Rare:77 | ||||
| chr9:133030925-133031017 | Rare:35 | ||||
| chr9:133336098-133336386 | Common:1; Rare:134 | ||||
| chr9:133347992-133348253 | Common:3; Rare:90 | ||||
| chr9:133356443-133356636 | Common:1; Rare:92; Clinvar (benign):2 | ||||
| chr9:133376017-133376368 | Common:1; Rare:125 | ||||
| chr9:133417917-133418368 | Common:4; Rare:115 |