| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322729-128322914 | Common:2; Rare:88; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr9:128340433-128340712 | Common:2; Rare:88 | ||||
| chr9:128371199-128371395 | Rare:71 | ||||
| chr9:128455950-128456203 | Common:1; Rare:82 | ||||
| chr9:128504581-128504806 | Rare:105; Clinvar:5 | ||||
| chr9:128552388-128552641 | Rare:100; Clinvar:5 | ||||
| chr9:128656656-128657051 | Common:2; Rare:120; Clinvar (pathogenic):1 | ||||
| chr9:128683603-128683891 | Rare:66 | ||||
| chr9:128724095-128724467 | Common:2; Rare:123 | ||||
| chr9:128771854-128771980 | Rare:35 | ||||
| chr9:128787147-128787341 | Common:3; Rare:66 | ||||
| chr9:128881887-128882207 | Common:2; Rare:101 | ||||
| chr9:128882475-128882641 | Common:1; Rare:45 | ||||
| chr9:128922004-128922320 | Common:1; Rare:73 |