| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127937832-127937977 | Common:2; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:128160046-128160410 | Common:2; Rare:90 | ||||
| chr9:128191806-128191844 | Rare:8 | ||||
| chr9:128275933-128276320 | Common:5; Rare:182 | ||||
| chr9:128322410-128322485 | Rare:30 | ||||
| chr9:128371193-128371383 | Rare:63 | ||||
| chr9:128504601-128504747 | Rare:63; Clinvar:3 | ||||
| chr9:128552408-128552611 | Rare:79; Clinvar:1 | ||||
| chr9:128656646-128657051 | Common:2; Rare:123; Clinvar (pathogenic):1 | ||||
| chr9:128724070-128724467 | Common:2; Rare:135 | ||||
| chr9:128771860-128772024 | Rare:39 | ||||
| chr9:128921988-128922314 | Common:1; Rare:75 | ||||
| chr9:128947604-128947725 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129139901-129140124 | Rare:44 | ||||
| chr9:129835228-129835481 | Common:2; Rare:100 |