chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108285711282857113CT29GENIChomozygous953085834
108286236582862366GA33GENIChomozygous953085835
108286310982863110AG31GENIChomozygous953085836
108286317982863180CT33GENIChomozygous953085837
108286342382863424TG31GENIChomozygous953085838
108286370182863702GT22GENIChomozygous953085839
108286490782864908TC20GENIChomozygous953085840
108286496682864967AT24GENIChomozygous953085841
108286515682865157TA19GENIChomozygous953085842
108286541782865418AT31GENIChomozygous953085843
108286551382865514AG33GENIChomozygous953085844
108286568482865685AG19GENIChomozygous953085845
108286574582865746GA32GENIChomozygous953085846
108286601382866014TA25GENIChomozygous953085847
108286657682866577GA19GENIChomozygous953085848
108286668982866690GA8GENIChomozygous953085849
108286678882866789GA21GENIChomozygous953085850
108286726182867262CT21GENIChomozygous953085851
108286734482867345TC18GENIChomozygous953085852
108286779682867797GA21GENIChomozygous953085853
108286803682868037CA37GENIChomozygous953085854
108286844082868441GA29GENIChomozygous953085855
108286876782868768CT22GENIChomozygous953085856
108286934082869341CT18GENIChomozygous953085857
108286952682869527AC22GENIChomozygous953085858
108286971082869711TC20GENICpossibly homozygous953085859
108287094482870945GC18GENIChomozygous953085860
108287096382870964GC18GENIChomozygous953085861
108288769582887696CG5GENIChomozygous953085862