| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129835217-129835498 | Common:3; Rare:111 | ||||
| chr9:130043086-130043334 | Common:2; Rare:85 | ||||
| chr9:130053854-130054007 | Common:1; Rare:63 | ||||
| chr9:130579461-130579674 | Common:5; Rare:87 | ||||
| chr9:131502900-131503062 | Rare:60; Clinvar:3 | ||||
| chr9:131531182-131531363 | Common:9; Rare:82 | ||||
| chr9:132354936-132355147 | Common:3; Rare:65 | ||||
| chr9:132406814-132406885 | Rare:24 | ||||
| chr9:132669937-132670057 | Common:1; Rare:56 | ||||
| chr9:132878272-132878385 | Common:1; Rare:41 | ||||
| chr9:133030457-133030752 | Common:4; Rare:81 | ||||
| chr9:133348025-133348260 | Common:3; Rare:92 | ||||
| chr9:133348813-133349036 | Rare:82 | ||||
| chr9:133356436-133356648 | Common:1; Rare:102; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375999-133376404 | Common:3; Rare:146 |