chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175398329053983291CT10GENIChomozygous111247711
175398448153984482TC11GENIChomozygous111063710
175398519453985195AC17GENIChomozygous111063711
175398725053987251AG9GENIChomozygous111063712
175399013353990134TC18GENIChomozygous111352386
175399312053993121AC16GENIChomozygous111247713
175399347153993472GC22GENIChomozygous111247715
175399390753993908GA26GENIChomozygous111247717
175399448553994486GA30GENIChomozygous111247719
175399836253998363AT24GENIChomozygous111063724
175400060254000603AT11GENIChomozygous111247721
175400221054002211TA15GENIChomozygous111063732
175400437254004373AG25GENIChomozygous111063734
175400458654004587CA20GENIChomozygous111247725
175400539354005394AG6GENIChomozygous111247727
175400976554009766GA22GENIChomozygous111247729
175401080154010802AG30GENIChomozygous111063753
175401097654010977CT17GENIChomozygous111247731
175401238554012386TC19GENIChomozygous111247733
175401771154017712CT24GENIChomozygous111063769
175401795154017952TC10GENIChomozygous111063770
175401848354018484CT16GENIChomozygous111247735
175402255854022559AG24GENIChomozygous111247737
175402314954023150CT15GENIChomozygous111247739
175402457954024580CT16GENIChomozygous111247741
175402475754024758AG15GENIChomozygous111063786