chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56478954364789544GA28GENICpossibly homozygous113835685
56479085264790853TC24GENIChomozygous113835686
56479093464790935AC37GENIChomozygous113835687
56479160264791603TA33GENIChomozygous113835688
56479185864791859GA30GENIChomozygous113835689
56479235364792354CT12GENIChomozygous113835690
56479389164793892GA71GENICheterozygous113835691
56479397964793980GT69GENICheterozygous113835692
56479407364794074TC66GENICheterozygous113835693
56479411064794111TC37GENICheterozygous113835694
56479432364794324CT7GENIChomozygous113835695
56479467964794680CT22GENIChomozygous113835696
56479471864794719AG19GENIChomozygous113835697
56479535564795356TC28GENIChomozygous113835698
56479568264795683AG28GENIChomozygous113835699
56479590964795910GA8GENIChomozygous113835700
56479611064796111AG11GENIChomozygous113835701
56479671564796716AG29GENIChomozygous113835702
56479698564796986AG23GENIChomozygous113835703
56479954464799545CT29GENIChomozygous113835704
56479979064799791AG21GENIChomozygous113835705
56480024064800241GC36GENIChomozygous113835706