chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113078107430781075AT44GENIChomozygous145764759
113078108730781088AT43GENIChomozygous145764760
113078172430781725TC43GENIChomozygous142282736
113078179030781792TC36GENIChomozygous145753267
113078179330781794GA37GENIChomozygous145764761
113078182530781826AG36GENIChomozygous138952983
113078233230782333AC43GENIChomozygous138952984
113078278730782788AG57GENIChomozygous138952985
113078384430783845AG46GENIChomozygous138952986
113078396630783966CT47GENIChomozygous138880799
113078462730784628AG40GENIChomozygous138952987
113078478630784787C29GENIChomozygous138880800
113078602530786026TC50GENIChomozygous138952988
113078610730786108CG29GENIChomozygous138952989
113078663930786640AG51GENIChomozygous138952990
113078673030786731CG46GENIChomozygous138952991
113078697330786974AG54GENIChomozygous138952992
113078766830787669G45GENIChomozygous138880801
113078800730788008TC40GENIChomozygous138952993
113078819130788192CT48GENIChomozygous138952994
113078831030788311TC43GENIChomozygous138952995
113079016930790170CT59GENIChomozygous145764762
113079062530790629CACA48GENIChomozygous138880802
113079084530790846AG40GENIChomozygous138952997
113079111430791115CA23GENIChomozygous138952998
113079172430791725GA45GENIChomozygous138952999
113079209130792092TA47GENIChomozygous138953000
113079241530792416T43GENICpossibly homozygous138880803
113079259530792596TA39GENIChomozygous138953002
113079298930792990GA37GENIChomozygous138953005
113079367730793678CT43GENIChomozygous138953006
113079469930794700GT44GENICpossibly homozygous138953007
113079548830795489GA38GENIChomozygous138953008
113079614730796148GA38GENIChomozygous145764763
113079681030796811GA54GENIChomozygous145764764
113079702330797024TA32GENIChomozygous138953010
113079748330797484GA47GENIChomozygous138953012
113079758430797586AG46GENIChomozygous145753268
113079769530797696AG50GENIChomozygous138953013