| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122264799-122264919 | Common:1; Rare:34 | ||||
| chr9:127451355-127451520 | Common:2; Rare:64 | ||||
| chr9:127877667-127877767 | Rare:18 | ||||
| chr9:128275936-128276302 | Common:5; Rare:170 | ||||
| chr9:128322414-128322607 | Common:1; Rare:56 | ||||
| chr9:128552413-128552589 | Rare:67; Clinvar:1 | ||||
| chr9:128656652-128657002 | Common:2; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:128724095-128724464 | Common:2; Rare:121 | ||||
| chr9:128947598-128947725 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129110671-129110953 | Common:3; Rare:64 | ||||
| chr9:129835228-129835481 | Common:2; Rare:100 | ||||
| chr9:130053854-130053934 | Common:1; Rare:25 | ||||
| chr9:130693626-130693786 | Rare:51 | ||||
| chr9:132669974-132670039 | Common:1; Rare:33 | ||||
| chr9:133348080-133348258 | Common:1; Rare:74 |