| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128693978-128694141 | Common:1; Rare:46 | ||||
| chr9:128748095-128748265 | Common:2; Rare:28 | ||||
| chr9:128750581-128750623 | Rare:15 | ||||
| chr9:128883039-128883198 | Common:1; Rare:42 | ||||
| chr9:128945954-128946313 | Rare:121; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr9:128946357-128946590 | Rare:77; Clinvar:5; Clinvar (benign):4 | ||||
| chr9:129010783-129010827 | Common:1; Rare:15 | ||||
| chr9:129011143-129011334 | Rare:50 | ||||
| chr9:129167717-129167815 | Rare:18 | ||||
| chr9:129176695-129177023 | Common:3; Rare:116 | ||||
| chr9:129177327-129177701 | Common:2; Rare:145 | ||||
| chr9:129488992-129489197 | Common:1; Rare:37 | ||||
| chr9:129496731-129496932 | Common:2; Rare:59 | ||||
| chr9:129504486-129504617 | Rare:23 | ||||
| chr9:129575566-129575688 | Rare:24 |