chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT21GENIChomozygous876950709
5159590355159590356AC8GENIChomozygous876950710
5159590356159590357GC6GENIChomozygous876950711
5159590377159590378GA10GENIChomozygous876950712
5159590516159590517AG16GENIChomozygous876950713
5159590543159590544TC21GENIChomozygous876950714
5159590567159590568TC13GENIChomozygous876950715
5159591041159591042CT29GENIChomozygous876950716
5159591165159591166AG26GENIChomozygous876950717
5159591294159591295GA19GENIChomozygous876950718
5159591492159591493CT18GENIChomozygous876950719
5159591711159591712GA19GENIChomozygous876950720
5159591959159591960CT21GENIChomozygous876950721
5159592241159592242AG17GENIChomozygous876950722
5159592551159592552GA30GENIChomozygous876950723
5159592593159592594GA25GENIChomozygous876950724
5159592713159592714CT13GENIChomozygous876950725
5159593011159593012TA11GENIChomozygous876950726
5159593229159593230AG17GENIChomozygous876950727
5159593316159593317AC17GENIChomozygous876950728
5159594481159594482GA19GENIChomozygous876950729
5159595521159595522GA17GENIChomozygous876950730
5159598268159598269GA20GENIChomozygous876950731
5159599504159599505TC28GENIChomozygous876950732
5159600471159600472TC20GENIChomozygous876950733
5159601143159601144CT29GENIChomozygous876950734
5159601217159601218AG15GENIChomozygous876950735
5159601274159601275AG26GENIChomozygous876950736
5159602018159602019CT12GENIChomozygous876950737