chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155675687856756879AG10GENIChomozygous112989889
155675836956758370CT25GENIChomozygous112989890
155675866756758668AC13GENIChomozygous112518306
155676423156764232AG26GENIChomozygous112518316
155676497156764972AG18GENIChomozygous112518318
155676535356765354AT14GENIChomozygous112518320
155676559756765598AG16GENIChomozygous112518324
155676678456766785GA31GENIChomozygous112989891
155676803156768032TG13GENIChomozygous112518334
155676871856768719CT31GENIChomozygous112518336
155676961856769619AG26GENIChomozygous112918491
155677035356770354TC28GENIChomozygous112689004
155677053356770534TA18GENIChomozygous112918495
155677102856771029GA28GENIChomozygous112989892
155677149056771491CT16GENIChomozygous112989893
155677297656772977CT31GENIChomozygous112918497
155677386656773867CT16GENIChomozygous112918499
155677399556773996CT36GENIChomozygous112918501
155677411856774119AT22GENIChomozygous112918503
155677411956774120AC24GENIChomozygous112918505
155677414356774144GA27GENIChomozygous112989894
155677450156774502GA21GENIChomozygous112918507
155677532956775330TA24GENIChomozygous112989895
155677591756775918TC27GENIChomozygous112918509
155677615456776155TC36GENIChomozygous112689008
155677583556775836CT37GENIChomozygous112989897
155677540956775410CT29GENIChomozygous112989896