| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129803053-129803194 | Common:2; Rare:43 | ||||
| chr9:129824093-129824299 | Common:3; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:129835232-129835481 | Common:2; Rare:96 | ||||
| chr9:130053854-130053933 | Common:1; Rare:24 | ||||
| chr9:130835171-130835464 | Common:11; Rare:104 | ||||
| chr9:131125425-131125637 | Common:2; Rare:98 | ||||
| chr9:131502859-131503016 | Rare:58; Clinvar:3 | ||||
| chr9:131531126-131531359 | Common:9; Rare:104 | ||||
| chr9:132669930-132670046 | Common:1; Rare:55 | ||||
| chr9:133030509-133030743 | Common:3; Rare:59 | ||||
| chr9:133348039-133348258 | Common:2; Rare:86 | ||||
| chr9:133348808-133349042 | Rare:85 | ||||
| chr9:133356452-133356630 | Common:1; Rare:84; Clinvar (benign):2 | ||||
| chr9:133375995-133376377 | Common:3; Rare:138 | ||||
| chr9:134641551-134641809 | Common:2; Rare:80; Clinvar (benign):1 |