| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129098247-129098575 | Rare:90 | ||||
| chr9:129110474-129110581 | Rare:26 | ||||
| chr9:129110605-129110962 | Common:4; Rare:81 | ||||
| chr9:129139901-129140138 | Rare:48 | ||||
| chr9:129818522-129818751 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr9:129835210-129835490 | Common:2; Rare:113 | ||||
| chr9:130043074-130043336 | Common:2; Rare:89 | ||||
| chr9:130053847-130053939 | Common:1; Rare:30 | ||||
| chr9:130451928-130452333 | Common:2; Rare:117; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr9:130579442-130579740 | Common:7; Rare:114 | ||||
| chr9:131125407-131125667 | Common:2; Rare:123 | ||||
| chr9:131531120-131531357 | Common:9; Rare:105 | ||||
| chr9:132354932-132355248 | Common:4; Rare:104 | ||||
| chr9:132669936-132670051 | Common:1; Rare:54 | ||||
| chr9:132878264-132878394 | Common:1; Rare:49 |