| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124861883-124862125 | Rare:107 | ||||
| chr9:124940961-124941168 | Common:3; Rare:72 | ||||
| chr9:125241312-125241686 | Common:3; Rare:114 | ||||
| chr9:125261716-125261846 | Common:1; Rare:47 | ||||
| chr9:127451325-127451520 | Common:2; Rare:83 | ||||
| chr9:127937826-127938007 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:128275922-128276293 | Common:4; Rare:166 | ||||
| chr9:128322410-128322485 | Rare:30 | ||||
| chr9:128371195-128371383 | Rare:63 | ||||
| chr9:128504601-128504774 | Rare:78; Clinvar:5 | ||||
| chr9:128552408-128552612 | Rare:79; Clinvar:1 | ||||
| chr9:128724088-128724480 | Common:4; Rare:128 | ||||
| chr9:128947598-128947725 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129753028-129753177 | Rare:39 | ||||
| chr9:129835232-129835481 | Common:2; Rare:96 |