chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126196656126196657GA17GENIChomozygous113996640
5126198484126198485GT24GENIChomozygous113996642
5126198694126198695AG42GENIChomozygous113996644
5126206686126206687AT34GENIChomozygous113996652
5126208062126208063CT17GENIChomozygous113996654
5126208247126208248GT26GENIChomozygous113996656
5126208411126208412GA31GENIChomozygous113996658
5126208590126208591TA27GENIChomozygous113996660
5126209139126209140GA20GENIChomozygous113996662
5126209608126209609AG24GENIChomozygous113996664
5126209611126209612GA24GENIChomozygous113996666
5126209705126209706TC24GENIChomozygous113996668
5126209708126209709GA23GENIChomozygous113996670
5126209715126209716GC25GENIChomozygous113996672
5126209768126209769CA34GENICpossibly homozygous113996674
5126210065126210066TA27GENIChomozygous113996675
5126210514126210515AG30GENIChomozygous113996677
5126210631126210632TA34GENIChomozygous113996679
5126210873126210874TC31GENIChomozygous113996681
5126211601126211602CA23GENIChomozygous113996683
5126212657126212658CT22GENIChomozygous113996685
5126212671126212672AG22GENIChomozygous113996687
5126215100126215101GA27GENIChomozygous113996689
5126216747126216748CT10GENIChomozygous113996691
5126218232126218233CT39GENIChomozygous113996693
5126219108126219109AC38GENIChomozygous113996695
5126219778126219779TC17GENIChomozygous113996697
5126220266126220267CT25GENIChomozygous113996699
5126220467126220468AC24GENIChomozygous113996701