chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52957396529573966GA10GENIChomozygous113709044
52957589529575896CT18GENIChomozygous114187744
52957757129577572TG14GENIChomozygous113709057
52957757229577573TC14GENIChomozygous113709058
52957909229579093AG35GENIChomozygous114187745
52957994729579948CT36GENIChomozygous113709063
52957621129576212CT38GENIChomozygous118879940
52957730329577304GA7GENIChomozygous118879942
52958081629580817TC17GENIChomozygous114395520
52958174829581749TC23GENIChomozygous114395522
52958191429581915CT34GENIChomozygous118879944
52958236429582365CT36GENIChomozygous114395524
52958243829582439AG25GENIChomozygous113709066
52958319029583191CT29GENIChomozygous114395528
52958327929583280GA24GENIChomozygous114395530
52958368029583681CT30GENIChomozygous114395532
52958410629584107GC19GENIChomozygous114395534
52958492929584930GA19GENIChomozygous118879946
52958503729585038CT27GENIChomozygous114395542
52958503829585039TG27GENIChomozygous114395544
52958521329585214CA29GENIChomozygous118879948
52958532829585329CT24GENIChomozygous114395550
52958536329585364CT28GENIChomozygous118879950
52958572429585725AG30GENICpossibly homozygous114395554
52958637129586372GA26GENIChomozygous118879952
52958657229586573TC27GENIChomozygous118879954
52958672029586721CT19GENIChomozygous113709069
52958881929588820CT38GENIChomozygous114187755
52959025229590253CG26GENIChomozygous118879956
52959272029592721CT28GENIChomozygous118879958
52959312429593125AG33GENIChomozygous113709072
52959354029593541CT48GENIChomozygous118879960
52959415629594157TC45GENIChomozygous113709073
52960025129600252TC16GENIChomozygous118879962
52960064929600650TC12GENIChomozygous113709075
52960099529600996AG9GENIChomozygous113709076