| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128787140-128787372 | Common:3; Rare:80 | ||||
| chr9:128881901-128882182 | Common:1; Rare:90 | ||||
| chr9:128947533-128947745 | Common:2; Rare:98; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:129036374-129036678 | Common:2; Rare:86 | ||||
| chr9:129110628-129110956 | Common:4; Rare:75 | ||||
| chr9:129111313-129111610 | Common:3; Rare:76 | ||||
| chr9:129628261-129628501 | Common:1; Rare:36 | ||||
| chr9:129803053-129803195 | Common:2; Rare:43 | ||||
| chr9:129823987-129824276 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:129835111-129835492 | Common:3; Rare:148 | ||||
| chr9:130042953-130043011 | Rare:10 | ||||
| chr9:130043018-130043291 | Common:2; Rare:83 | ||||
| chr9:130053801-130053970 | Common:1; Rare:62 | ||||
| chr9:130172229-130172521 | Common:2; Rare:72 | ||||
| chr9:130579442-130579760 | Common:7; Rare:120 |