chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89655176996551770CG29GENIChomozygous803706746
89655188596551886GA19GENIChomozygous803706747
89655217896552179GA51GENICheterozygous803706748
89655220196552202TC46GENICheterozygous803706749
89655242196552422GC19GENIChomozygous803706750
89655296696552967TG14GENIChomozygous803706751
89655352896553529TC7GENIChomozygous803706752
89655356696553567GA5GENIChomozygous803706753
89655385296553853TC8GENIChomozygous803706754
89655454496554545AG6GENIChomozygous803706755
89655533696555337TG18GENICpossibly homozygous803706756
89655576096555761CT13GENICpossibly homozygous803706757
89655601896556019CT10GENIChomozygous803706758
89655667896556679TC24GENIChomozygous803706759
89655763596557636GA24GENIChomozygous803706760
89655813296558133TC14GENIChomozygous803706761
89655821896558219TC28GENICheterozygous803706762