chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2051753365175337CG20GENIChomozygous109077614
2051754325175433CT19GENIChomozygous109077616
2051757465175747CA18GENIChomozygous109077618
2051757875175788CG7GENIChomozygous109077620
2051758065175807AG5GENIChomozygous109329688
2051758965175897AG8GENIChomozygous109077622
2051759045175905AG8GENIChomozygous109329690
2051764115176412TC2GENIChomozygous109296883
2051764195176420TC1GENIChomozygous109329692
2051773375177338GC11GENIChomozygous109077634
2051776545177655TG9GENIChomozygous109077644
2051776645177665GA10GENIChomozygous109077646
2051776755177676GA9GENIChomozygous109077648
2051778005177801GC18GENIChomozygous109077650
2051778305177831TC17GENIChomozygous109077652
2051780965178097TC25GENIChomozygous109077654
2051781345178135TA34GENIChomozygous109077656
2051782165178217GA28GENIChomozygous109077658
2051782395178240TC28GENIChomozygous109077660
2051783545178355GC17GENIChomozygous109077662
2051783645178365AG15GENIChomozygous109077664
2051785045178505GA22GENIChomozygous109077666
2051785235178524AG20GENIChomozygous109077668
2051785755178576AG18GENIChomozygous109077670
2051786395178640TC23GENIChomozygous109233919
2051786475178648AG23GENIChomozygous109233920
2051786755178676TA15GENIChomozygous109077672
2051788765178877GA18GENIChomozygous109077674
2051788835178884TG19GENIChomozygous109077676
2051789125178913AG20GENIChomozygous109077678
2051791005179101CT27GENIChomozygous109077680
2051792485179249GA24GENIChomozygous109077682