chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
179625970096259701TC16GENIChomozygous64791687
179625976596259766GA16GENIChomozygous64791689
179625989396259894CA20GENIChomozygous64791691
179626099996261000GC18GENIChomozygous64791693
179626145996261460TC26GENIChomozygous64791695
179626256396262564TC14GENIChomozygous64662760
179626501196265012AG26GENIChomozygous64662763
179626890896268909GT29GENIChomozygous65002248
179627050296270503GT25GENIChomozygous64791697
179627099496270995AC25GENICpossibly homozygous64791699
179627249096272491TG7GENIChomozygous64662772
179627499596274996AG26GENIChomozygous64662775
179627692196276922GA34GENIChomozygous64791701
179627702596277026CA33GENIChomozygous64791703
179627886496278865TC19GENIChomozygous64791705
179628063896280639TC37GENIChomozygous64662778
179628102696281027CG34GENICpossibly homozygous64791707
179628141596281416GA25GENICpossibly homozygous64791709
179628205296282053CG23GENICheterozygous64791711
179628205696282057CG23GENICheterozygous64791713
179628299296282993AG26GENIChomozygous64791719
179628345496283455GA26GENICpossibly homozygous64791721
179628349596283496AG24GENICpossibly homozygous64791723
179628350296283503AG23GENICpossibly homozygous64791725
179628852396288524TC20GENIChomozygous64791727
179629416896294169AG41GENIChomozygous64662789
179629466296294663GA26GENIChomozygous64791729
179629619896296199GA17GENIChomozygous64791731
179629653196296532CG28GENIChomozygous64791733
179629681396296814GA30GENIChomozygous64791735
179629834496298345AG24GENIChomozygous64791737
179629915196299152TC39GENIChomozygous64791739
179629946496299465GA23GENIChomozygous64791741
179630173296301733CT24GENIChomozygous64791743
179630185096301851GA24GENICpossibly homozygous64791745
179630312696303127GA33GENIChomozygous64791747
179631028796310288TC31GENIChomozygous64791749
179631151596311516TC37GENICpossibly homozygous64791751
179631323396313234CT30GENIChomozygous64791753
179631359196313592GA18GENIChomozygous64791755