| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130053847-130053944 | Common:1; Rare:33 | ||||
| chr9:130579445-130579683 | Common:7; Rare:101 | ||||
| chr9:130693493-130693808 | Rare:91 | ||||
| chr9:130835165-130835464 | Common:11; Rare:105 | ||||
| chr9:131125446-131125661 | Common:1; Rare:104 | ||||
| chr9:132354955-132355196 | Common:3; Rare:77 | ||||
| chr9:132409933-132410259 | Common:4; Rare:85 | ||||
| chr9:132669939-132670046 | Common:1; Rare:52 | ||||
| chr9:132878272-132878418 | Common:1; Rare:57 | ||||
| chr9:133129220-133129319 | Common:1; Rare:32 | ||||
| chr9:133163901-133164040 | Common:3; Rare:34 | ||||
| chr9:133275181-133275318 | Rare:29 | ||||
| chr9:133348039-133348268 | Common:2; Rare:93 | ||||
| chr9:133356425-133356630 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133376010-133376340 | Common:1; Rare:121 |