chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37206221572062216CA38GENIChomozygous811478855
37206255872062559GA21GENIChomozygous811478856
37206372472063725AG18GENIChomozygous811478857
37206425472064255AG18GENIChomozygous811478858
37206460372064604CT28GENIChomozygous811478859
37206494472064945CA31GENIChomozygous811478860
37206638972066390AG15GENIChomozygous811478861
37206679972066800CG34GENIChomozygous811478862
37206720772067208CT26GENIChomozygous811478863
37206726272067263CT27GENICpossibly homozygous811478864
37206733372067334CT10GENIChomozygous811478865
37206734572067346GT7GENIChomozygous811478866
37206743872067439GA11GENICheterozygous811478867
37206747872067479CT18GENIChomozygous811478868
37206765072067651GA25GENIChomozygous811478869
37206824472068245AG43GENIChomozygous811478870
37206827772068278AG34GENIChomozygous811478871
37206839472068395TC28GENIChomozygous811478872
37206998972069990GC35GENIChomozygous811478873
37207007172070072GA22GENIChomozygous811478874
37207046172070462CT23GENICheterozygous811478875