| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125200461-125200590 | Rare:49 | ||||
| chr9:125241270-125241656 | Common:2; Rare:115 | ||||
| chr9:125261691-125261848 | Common:1; Rare:62 | ||||
| chr9:126804928-126805060 | Common:1; Rare:39 | ||||
| chr9:127424247-127424488 | Common:1; Rare:80 | ||||
| chr9:127451257-127451533 | Common:2; Rare:121 | ||||
| chr9:127612047-127612318 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127877667-127877790 | Rare:23 | ||||
| chr9:128169404-128169741 | Rare:93; Clinvar:2 | ||||
| chr9:128191515-128191651 | Rare:35 | ||||
| chr9:128275909-128276293 | Common:4; Rare:167 | ||||
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322739-128322906 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:128371202-128371395 | Rare:71 | ||||
| chr9:128504601-128504752 | Rare:64; Clinvar:3 |