| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129110619-129111029 | Common:5; Rare:126 | ||||
| chr9:129835159-129835498 | Common:4; Rare:132 | ||||
| chr9:130043100-130043304 | Common:2; Rare:64 | ||||
| chr9:130053854-130053978 | Common:1; Rare:52 | ||||
| chr9:131125446-131125651 | Common:1; Rare:99 | ||||
| chr9:131502885-131503012 | Rare:45; Clinvar:3 | ||||
| chr9:131531174-131531336 | Common:9; Rare:73 | ||||
| chr9:131709817-131709981 | Rare:32 | ||||
| chr9:132669936-132670079 | Common:1; Rare:65 | ||||
| chr9:132878286-132878430 | Common:1; Rare:55 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133336083-133336330 | Common:1; Rare:112 | ||||
| chr9:133348024-133348246 | Common:3; Rare:81 | ||||
| chr9:133356425-133356618 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375965-133376332 | Common:3; Rare:134 |