chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52937572829375729AG16GENIChomozygous137409689
52937575729375758AT21GENIChomozygous141710816
52937593729375938TA11GENIChomozygous137409690
52937595929375960GC10GENIChomozygous141710817
52937645229376453TC19GENIChomozygous137409691
52937659929376600T9GENICpossibly homozygous144695975
52937661529376616AG15GENIChomozygous137409692
52937665129376653AT13GENIChomozygous137297530
52937698229376982T17GENIChomozygous137297531
52937699229376992T18GENIChomozygous137297532
52937778129377782CT19GENIChomozygous137409693
52937841129378412GA15GENIChomozygous141710818
52937869629378697GT26GENIChomozygous137409694
52938186629381867CT25GENIChomozygous141710819
52938856729388568GA17GENIChomozygous137409702
52938419129384191T16GENIChomozygous141679145
52938966329389664CT24GENIChomozygous137409704
52939189229391893GA20GENIChomozygous141710820
52939445329394454TC23GENIChomozygous137409708
52939745229397453CT18GENIChomozygous141710821
52940110729401108AG20GENIChomozygous137409719
52940206729402068AG13GENIChomozygous141710822
52940226429402265AC20GENIChomozygous141710823
52940236029402361AG16GENIChomozygous137409728
52940240429402405TG14GENIChomozygous141710825
52938188629381887CA25GENIChomozygous154274576
52938188629381887C25GENICheterozygous403136950