| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128260718-128260910 | Common:3; Rare:48 | ||||
| chr9:128275900-128276327 | Common:5; Rare:191 | ||||
| chr9:128322402-128322621 | Common:1; Rare:66 | ||||
| chr9:128322729-128323028 | Common:3; Rare:137; Clinvar:3; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr9:128371184-128371407 | Rare:83 | ||||
| chr9:128552408-128552693 | Rare:111; Clinvar:6; Clinvar (benign):3 | ||||
| chr9:128625935-128626153 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:128630123-128630330 | Common:3; Rare:55; Clinvar (benign):2 | ||||
| chr9:128683177-128683544 | Common:6; Rare:53 | ||||
| chr9:128683667-128683939 | Rare:73 | ||||
| chr9:128724046-128724467 | Common:2; Rare:152 | ||||
| chr9:128771854-128772067 | Common:2; Rare:65 | ||||
| chr9:128881901-128882243 | Common:2; Rare:118 | ||||
| chr9:128922000-128922356 | Common:2; Rare:87 | ||||
| chr9:128947531-128947722 | Common:1; Rare:85; Clinvar:5; Clinvar (benign):1 |