| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127579003-127579305 | Common:4; Rare:60 | ||||
| chr9:127877654-127877770 | Rare:26 | ||||
| chr9:128160045-128160414 | Common:2; Rare:91 | ||||
| chr9:128191515-128191699 | Common:1; Rare:49 | ||||
| chr9:128259007-128259296 | Common:1; Rare:78 | ||||
| chr9:128275900-128276293 | Common:4; Rare:171 | ||||
| chr9:128322414-128322632 | Common:1; Rare:59 | ||||
| chr9:128322729-128322856 | Common:2; Rare:46; Clinvar (benign):5 | ||||
| chr9:128371196-128371425 | Rare:89 | ||||
| chr9:128552394-128552636 | Rare:96; Clinvar:5 | ||||
| chr9:128608890-128609273 | Rare:104; Clinvar:5; Clinvar (benign):11 | ||||
| chr9:128656620-128656825 | Common:2; Rare:96; Clinvar (pathogenic):1 | ||||
| chr9:128683634-128683912 | Rare:72 | ||||
| chr9:128684956-128685093 | Rare:25 | ||||
| chr9:128689426-128689651 | Rare:77 |