chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46860724168607242AT19GENIChomozygous112691663
46861608768616087G16GENIChomozygous128045641
46861614968616150G17GENIChomozygous128045642
46861618368616184C20GENIChomozygous128045643
46861620168616201G20GENIChomozygous128045644
46861620568616206A18GENIChomozygous128045645
46861621768616218CT20GENIChomozygous112691681
46861623168616231C20GENIChomozygous128045646
46861626068616261AC22GENIChomozygous112691683
46861626968616269C22GENIChomozygous128045647
46861629668616296T22GENIChomozygous128045648
46861629868616299G22GENIChomozygous128045649
46861630668616307G22GENIChomozygous128045650
46861634168616342C24GENIChomozygous128045651
46861638368616384G19GENIChomozygous128045652
46861640368616404T18GENIChomozygous128045653
46861642668616426G20GENIChomozygous128045654
46861643568616435T20GENIChomozygous128045656
46861650568616506C19GENIChomozygous128045657
46861653468616534T18GENIChomozygous128045658
46861654368616544GT18GENIChomozygous112691685
46861658568616585C19GENIChomozygous128045659
46861659868616598T20GENIChomozygous128045660
46862120868621209C15GENIChomozygous128045661
46862125168621251G22GENIChomozygous128045662
46862144468621445C14GENIChomozygous128045663
46862163268621633GT17GENIChomozygous112691687
46862209868622099TC13GENIChomozygous112691689
46862540168625402CA20GENIChomozygous112691701
46861145568611456TA31GENIChomozygous119433005
46862647368626473C8GENIChomozygous132831862