chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73443108734431088TC7GENICpossibly homozygous54190130
73443143334431434TG13GENICpossibly homozygous54190138
73443211534432116CA1GENIChomozygous53869768
73443211934432120TA1GENIChomozygous53869769
73443212234432123CA1GENIChomozygous53869770
73443327934433280AG17GENICpossibly homozygous54190143
73443335934433360TC14GENICpossibly homozygous55924389
73444813134448132CG3GENIChomozygous54190146
73444813834448139TC4GENIChomozygous54190147
73446337234463373AG19GENIChomozygous55924391
73446503734465038GA10GENICpossibly homozygous55924393
73446582034465822CT--3GENIChomozygous54190162
73446908934469090AT4GENIChomozygous55924395
73447123034471231AT4GENICheterozygous54190195