chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175398329053983291CT11GENIChomozygous111247711
175398448153984482TC24GENIChomozygous111063710
175398519453985195AC10GENIChomozygous111063711
175398725053987251AG24GENIChomozygous111063712
175399312053993121AC14GENIChomozygous111247713
175399347153993472GC7GENIChomozygous111247715
175399390753993908GA14GENIChomozygous111247717
175399448553994486GA14GENIChomozygous111247719
175399836253998363AT12GENIChomozygous111063724
175400060254000603AT20GENIChomozygous111247721
175400402954004030GT19GENIChomozygous111247723
175400437254004373AG19GENIChomozygous111063734
175400458654004587CA19GENIChomozygous111247725
175400976554009766GA9GENIChomozygous111247729
175400357954003580CA17GENIChomozygous119391428
175401080154010802AG21GENIChomozygous111063753
175401097654010977CT15GENIChomozygous111247731
175401238554012386TC8GENIChomozygous111247733
175401650154016502GC7GENICheterozygous125548264
175401771154017712CT19GENIChomozygous111063769
175401795154017952TC27GENIChomozygous111063770
175401848354018484CT13GENIChomozygous111247735
175402255854022559AG20GENIChomozygous111247737
175402314954023150CT12GENIChomozygous111247739
175402457954024580CT7GENIChomozygous111247741
175402475754024758AG15GENIChomozygous111063786