| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127810756-127811002 | Rare:50 | ||||
| chr9:127816038-127816094 | Rare:20; Clinvar:1 | ||||
| chr9:127819621-127819753 | Rare:41; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr9:127826659-127826789 | Rare:35; Clinvar:1 | ||||
| chr9:127908511-127908721 | Common:1; Rare:51 | ||||
| chr9:128684439-128684559 | Rare:25 | ||||
| chr9:129005445-129005765 | Common:1; Rare:90 | ||||
| chr9:129175919-129176015 | Common:1; Rare:34 | ||||
| chr9:129320899-129321020 | Rare:17 | ||||
| chr9:129334181-129334257 | Rare:16 | ||||
| chr9:129334408-129334702 | Rare:70 | ||||
| chr9:129344013-129344028 | Rare:1 | ||||
| chr9:129413723-129413960 | Common:3; Rare:100 | ||||
| chr9:129488517-129488857 | Common:2; Rare:91 | ||||
| chr9:129489034-129489145 | Common:1; Rare:17 |