| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128881902-128882234 | Common:2; Rare:112 | ||||
| chr9:128921970-128922324 | Common:1; Rare:78 | ||||
| chr9:128947549-128947716 | Common:1; Rare:79; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129110667-129110953 | Common:3; Rare:65 | ||||
| chr9:129139935-129140138 | Rare:42 | ||||
| chr9:129752892-129753182 | Common:2; Rare:95 | ||||
| chr9:129824081-129824327 | Common:4; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:129835218-129835486 | Common:2; Rare:109 | ||||
| chr9:130053847-130053939 | Common:1; Rare:30 | ||||
| chr9:130693502-130693805 | Rare:88 | ||||
| chr9:130835160-130835397 | Common:8; Rare:79 | ||||
| chr9:131125405-131125637 | Common:2; Rare:106 | ||||
| chr9:131502860-131503012 | Rare:56; Clinvar:3 | ||||
| chr9:131531171-131531340 | Common:9; Rare:77 | ||||
| chr9:132354922-132355200 | Common:3; Rare:90 |