chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108285711282857113CT19GENIChomozygous116812778
108285741782857418AG35GENIChomozygous116812780
108286236582862366GA19GENIChomozygous116812782
108286263182862632AG11GENIChomozygous116898555
108286310982863110AG23GENIChomozygous116812784
108286317982863180CT27GENIChomozygous116812786
108286370182863702GT10GENIChomozygous116812788
108286496682864967AT18GENIChomozygous116812794
108286515682865157TA31GENIChomozygous116659882
108286541782865418AT30GENIChomozygous116812796
108286551382865514AG33GENIChomozygous116812798
108286568482865685AG28GENIChomozygous116812800
108286574582865746GA40GENICpossibly homozygous116812802
108286601382866014TA20GENICpossibly homozygous116812804
108286657682866577GA35GENIChomozygous116812806
108286668982866690GA25GENIChomozygous116812808
108286678882866789GA24GENIChomozygous116812810
108286726182867262CT22GENIChomozygous116812812
108286734482867345TC29GENIChomozygous116812814
108286779682867797GA43GENICpossibly homozygous116812816
108286803682868037CA34GENIChomozygous116812818
108286876782868768CT31GENIChomozygous116812822
108286934082869341CT26GENIChomozygous116812824
108286952682869527AC25GENIChomozygous116659886
108286971082869711TC16GENIChomozygous116659888
108288397882883979CT18GENIChomozygous116812834
108288769582887696CG10GENIChomozygous116980623