| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128881936-128882206 | Common:2; Rare:93 | ||||
| chr9:128922004-128922320 | Common:1; Rare:73 | ||||
| chr9:128947578-128947728 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129110671-129110982 | Common:5; Rare:80 | ||||
| chr9:129835169-129835492 | Common:3; Rare:127 | ||||
| chr9:130043073-130043339 | Common:2; Rare:91 | ||||
| chr9:130053854-130053963 | Common:1; Rare:44 | ||||
| chr9:130579447-130579680 | Common:6; Rare:101 | ||||
| chr9:131096403-131096572 | Common:3; Rare:50 | ||||
| chr9:132354947-132355207 | Common:3; Rare:83 | ||||
| chr9:132669939-132670040 | Common:1; Rare:49 | ||||
| chr9:132878272-132878414 | Common:1; Rare:56 | ||||
| chr9:133348037-133348266 | Common:3; Rare:91 | ||||
| chr9:133348670-133349042 | Common:3; Rare:157 | ||||
| chr9:133356458-133356593 | Common:1; Rare:61; Clinvar (benign):2 |