chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2032329373232938TG47GENIChomozygous109370614
2032329413232942GA48GENIChomozygous109388863
2032329623232963GC60GENIChomozygous109370616
2032329773232978AC61GENICpossibly homozygous109068275
2032329993233000CG68GENIChomozygous109388864
2032330453233046AT39GENIChomozygous109388865
2032330843233085GA31GENIChomozygous109388866
2032330853233086CT31GENIChomozygous109388867
2032331393233140GT30GENIChomozygous109370620
2032332093233210AG32GENIChomozygous109370622
2032332123233213GT33GENIChomozygous109370624
2032332183233219CG33GENIChomozygous109416942
2032334103233411TA59GENICpossibly homozygous109388868
2032334603233461GC49GENIChomozygous109388869
2032335503233551TC24GENIChomozygous109370626
2032336413233642CA20GENIChomozygous109388870
2032337823233783CT9GENIChomozygous109370630
2032337973233798CT16GENIChomozygous109370632
2032339153233916AG45GENIChomozygous109388871
2032341183234119CA34GENIChomozygous109388874
2032343973234398TA67GENIChomozygous109388875
2032348713234872GT44GENIChomozygous109388882
2032348843234885CG45GENIChomozygous109461493
2032386543238655CA19GENIChomozygous109068279
2032386593238660AT25GENIChomozygous109370638
2032386903238691TG30GENIChomozygous109454619
2032387213238722AG33GENIChomozygous109370640