Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:62802005-62802068 | Rare:1 | ||||
chr9:62802628-62802781 | |||||
chr9:73158597-73158734 | Rare:47 | ||||
chr9:87728100-87728809 | Common:2; Rare:191 | ||||
chr9:107734663-107734863 | Common:3; Rare:39 | ||||
chr9:125238665-125238965 | Common:1; Rare:81 | ||||
chr9:129698654-129698762 | Rare:21 | ||||
chr9:136438931-136439099 | Rare:63; Clinvar (pathogenic):1 | ||||
chr9:136728159-136728331 | Common:2; Rare:76 | ||||
chr9:137223387-137223681 | Common:3; Rare:103 | ||||
chrM:260-839 | |||||
chrM:1667-1792 | |||||
chrM:1806-2655 | |||||
chrM:6519-6733 | |||||
chrM:6891-6981 |