chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2049380064938007CT17GENICheterozygous403462306
2049380064938007C17GENICheterozygous403462307
2049380084938009CT17GENICheterozygous403462308
2049380084938009C17GENICheterozygous403462309
2049380104938011CT17GENICheterozygous403462310
2049380104938011C17GENICheterozygous403462311
2049380124938013CT17GENICheterozygous403462312
2049380124938013C17GENICheterozygous403462313
2049387844938785GA76GENIChomozygous130034835
2049403894940390CA73GENIChomozygous130034836
2049408184940819GC58GENIChomozygous130034837
2049410294941030GC54GENIChomozygous130034838
2049413934941394CT61GENIChomozygous130034839
2049415054941506TC55GENIChomozygous130034840
2049432764943277TC55GENIChomozygous403462314
2049433964943397CT49GENIChomozygous403462315
2049433964943397C49GENICheterozygous403462316
2049421074942108AG65GENIChomozygous130034841
2049429844942985CT71GENIChomozygous130034842
2049430884943089AG64GENICpossibly homozygous130034843
2049432074943208TC48GENIChomozygous130034844
2049433904943391CG49GENIChomozygous130034845
2049434454943446AG47GENIChomozygous130034846
2049434464943447GC46GENIChomozygous130034847
2049435924943593AG50GENIChomozygous130034848
2049436754943676AG57GENIChomozygous130034849
2049438354943836TC51GENIChomozygous130034850
2049438414943842GA53GENIChomozygous130034851
2049440054944006GA46GENIChomozygous130034852
2049440154944016GT47GENIChomozygous130034853
2049440454944046AG44GENIChomozygous130034854
2049441064944107CT42GENIChomozygous130034855
2049441914944192TC54GENIChomozygous130034856
2049441964944197CT55GENIChomozygous130034857
2049450044945005AG51GENIChomozygous130034858
2049453344945335CT41GENIChomozygous130034859
2049454634945464GC51GENIChomozygous130034860
2049456044945605TC44GENIChomozygous130034861
2049457894945790AG48GENIChomozygous130034862
2049409214940921CCATGCCTGTCAGGAGAGCACACAGACAGCG51GENIChomozygous129980000
2049431754943175C52GENIChomozygous129980001
2049434174943417GC48GENIChomozygous129980002