chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47832057478320575AG48GENIChomozygous807146575
47832062078320621AC46GENIChomozygous807146576
47832063878320639CA55GENIChomozygous807146577
47832081578320816GA38GENIChomozygous807146578
47832140078321401TC45GENIChomozygous807146579
47832144778321448TA55GENIChomozygous807146580
47832274678322747CA44GENICpossibly homozygous807146581
47832291378322914TA50GENIChomozygous807146582
47832291878322919CA49GENIChomozygous807146583
47832306478323065CT53GENICpossibly homozygous807146584
47832315378323154GA67GENIChomozygous807146585
47832367778323678GA47GENIChomozygous807146586
47832382878323829TC59GENIChomozygous807146587
47832399678323997GA42GENIChomozygous807146588
47832419778324198CT52GENIChomozygous807146589
47832429778324298CT55GENIChomozygous807146590
47832433978324340GT40GENIChomozygous807146591
47832469278324693TA57GENIChomozygous807146592
47832473778324738GC56GENICpossibly homozygous807146593
47832505378325054AG55GENIChomozygous807146594
47832524978325250CT74GENIChomozygous807146595
47832595578325956AG55GENIChomozygous807146596
47832653078326531AG59GENIChomozygous807146597
47832659078326591AG60GENIChomozygous807146598
47832682978326830TC60GENIChomozygous807146599
47832691478326915AG53GENIChomozygous807146600
47832703778327038TC37GENICpossibly homozygous807146601