| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127877666-127877779 | Rare:22 | ||||
| chr9:127937826-127937883 | Common:1; Rare:18; Clinvar (benign):1 | ||||
| chr9:128091274-128091462 | Rare:37 | ||||
| chr9:128160061-128160420 | Common:2; Rare:88 | ||||
| chr9:128191750-128191773 | Rare:7 | ||||
| chr9:128275933-128276261 | Common:4; Rare:147 | ||||
| chr9:128322410-128322576 | Common:1; Rare:54 | ||||
| chr9:128322739-128322887 | Common:2; Rare:69; Clinvar (benign):5 | ||||
| chr9:128371225-128371395 | Rare:62 | ||||
| chr9:128552408-128552691 | Rare:111; Clinvar:6; Clinvar (benign):3 | ||||
| chr9:128656655-128657002 | Common:2; Rare:114; Clinvar (pathogenic):1 | ||||
| chr9:128689509-128689645 | Rare:53 | ||||
| chr9:128724102-128724464 | Common:2; Rare:116 | ||||
| chr9:128771877-128772008 | Rare:31 | ||||
| chr9:128787124-128787308 | Common:3; Rare:51 |