| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128921983-128922324 | Common:1; Rare:78 | ||||
| chr9:128947549-128947745 | Common:2; Rare:95; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:129110642-129110982 | Common:5; Rare:86 | ||||
| chr9:129111251-129111624 | Common:3; Rare:104 | ||||
| chr9:129835198-129835492 | Common:2; Rare:120 | ||||
| chr9:130043113-130043296 | Common:2; Rare:59 | ||||
| chr9:130053871-130053958 | Common:1; Rare:35 | ||||
| chr9:130579446-130579683 | Common:6; Rare:101 | ||||
| chr9:131125446-131125651 | Common:1; Rare:99 | ||||
| chr9:131502866-131503052 | Rare:66; Clinvar:3 | ||||
| chr9:131531160-131531350 | Common:9; Rare:85 | ||||
| chr9:132354936-132355208 | Common:3; Rare:85 | ||||
| chr9:132406813-132406920 | Rare:38 | ||||
| chr9:132669957-132670040 | Common:1; Rare:40 | ||||
| chr9:132878278-132878408 | Common:1; Rare:49 |