chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5169112372169112373TC59GENIChomozygous114087635
5169113004169113005AG60GENIChomozygous114087637
5169113592169113593TC43GENICpossibly homozygous114087639
5169113887169113888CT59GENICpossibly homozygous114087641
5169115300169115301AG53GENIChomozygous114087643
5169115376169115377GA64GENIChomozygous114087645
5169115492169115493GC59GENIChomozygous114087647
5169116064169116065CG61GENICpossibly homozygous114087649
5169116834169116835TG63GENIChomozygous114087651
5169116892169116893GA66GENICpossibly homozygous114087653
5169120090169120091TC44GENIChomozygous114087655
5169120957169120958CT43GENIChomozygous114087657
5169124594169124595GA63GENIChomozygous114087659
5169124839169124840GA60GENIChomozygous114087661
5169125431169125432AG91GENIChomozygous114087663
5169126222169126223AG44GENICpossibly homozygous114087665
5169127247169127248TC69GENIChomozygous114087667
5169129812169129813CT49GENICheterozygous114163055
5169129851169129852AG30GENIChomozygous114087669
5169130872169130873AG60GENICheterozygous114087671
5169130880169130881AG59GENICheterozygous114087673
5169136526169136527TC10GENIChomozygous114163056
5169136861169136862TC29GENIChomozygous114087675
5169138902169138903CT67GENIChomozygous114087677
5169140004169140005AG55GENIChomozygous114087679
5169141153169141154GA52GENIChomozygous114087681
5169141399169141400TC76GENIChomozygous114087683
5169141656169141657AG58GENIChomozygous114087685
5169145575169145576AG51GENICpossibly homozygous114087687
5169145723169145724CA44GENIChomozygous114087689
5169146433169146434AC38GENIChomozygous114087691
5169149393169149394AT63GENIChomozygous114087693
5169151436169151437AT57GENIChomozygous114087695
5169152739169152740AG76GENIChomozygous114087697