Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:124504727-124505105 | Common:7; Rare:109 | ||||
chr9:125239302-125239488 | Rare:43 | ||||
chr9:125485557-125485760 | Common:1; Rare:34 | ||||
chr9:125538186-125538305 | Rare:15 | ||||
chr9:125889616-125889919 | Common:1; Rare:80 | ||||
chr9:127448358-127448529 | Rare:73 | ||||
chr9:127495210-127495481 | Rare:66; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr9:128163872-128164120 | Rare:53 | ||||
chr9:128630246-128630342 | Common:2; Rare:23; Clinvar (benign):3 | ||||
chr9:128684429-128684559 | Rare:26 | ||||
chr9:129138761-129138840 | Common:1; Rare:18 | ||||
chr9:129320846-129321017 | Rare:26 | ||||
chr9:129413719-129413931 | Common:1; Rare:83 | ||||
chr9:129476912-129476980 | Common:1; Rare:16 | ||||
chr9:129483662-129483851 | Common:1; Rare:36 |