chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2039910653991066TG17GENIChomozygous109070779
2039911233991124AG17GENIChomozygous109070785
2039913163991317GC19GENIChomozygous109070793
2039914273991428CT18GENIChomozygous109070799
2039917693991770AC13GENIChomozygous109389229
2039918383991839CG14GENIChomozygous109389230
2039918823991883CA15GENIChomozygous109389231
2039922733992274AC16GENIChomozygous131559241
2039924253992426CT13GENIChomozygous131559242
2039923023992302A12GENIChomozygous131554686
2039926983992699CT10GENICpossibly homozygous129706123
2039927983992799CA3GENIChomozygous129706125
2039928003992801GT3GENIChomozygous131559243
2039928693992870GC2GENIChomozygous129706128