chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137640287076402871GA57GENIChomozygous139346960
137640296676402967AG39GENIChomozygous139346961
137640299676402997CT47GENIChomozygous139346962
137640307476403075AG59GENIChomozygous139346963
137640323576403236CG59GENIChomozygous139346964
137640334076403341GC49GENIChomozygous139346965
137640388176403882AG53GENIChomozygous139346966
137640440476404405TC46GENIChomozygous139346967
137640443676404437AT41GENIChomozygous139346968
137640446576404466CT44GENIChomozygous139346969
137640537476405375CT64GENICpossibly homozygous139346970
137640538276405383GA71GENICpossibly homozygous139346971
137640550576405506TC62GENIChomozygous139346972
137640619376406194TC61GENIChomozygous139346973
137640637776406378AG56GENIChomozygous139346974
137640647176406472CT57GENIChomozygous139346975
137640849576408496CT43GENIChomozygous139346976
137640880876408809AG51GENIChomozygous139346977
137640467476404675G65GENIChomozygous139185025
137640488976404889C67GENIChomozygous139185026
137640567676405691TGTTTGGCTCTCCCA35GENIChomozygous139185027
137640810276408102TG16GENIChomozygous139185028