| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124861908-124862125 | Rare:93 | ||||
| chr9:124940969-124941139 | Common:3; Rare:60 | ||||
| chr9:125241312-125241686 | Common:3; Rare:114 | ||||
| chr9:127122602-127122963 | Common:3; Rare:92 | ||||
| chr9:127424111-127424429 | Common:1; Rare:86 | ||||
| chr9:127451267-127451557 | Common:3; Rare:121; Clinvar (benign):1 | ||||
| chr9:127937824-127937896 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr9:128098278-128098544 | Common:1; Rare:55 | ||||
| chr9:128275919-128276288 | Common:4; Rare:165 | ||||
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322757-128322898 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:128371204-128371389 | Rare:64 | ||||
| chr9:128552408-128552611 | Rare:79; Clinvar:1 | ||||
| chr9:128683392-128683477 | Common:1; Rare:10 | ||||
| chr9:128724095-128724464 | Common:2; Rare:121 |