chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1104477431104477432GT30GENIChomozygous971585614
1104477450104477451GA33GENIChomozygous971585615
1104477451104477452AC31GENIChomozygous971585616
1104478219104478220CT28GENIChomozygous971585617
1104478304104478305CT32GENIChomozygous971585618
1104478470104478471GA30GENIChomozygous971585619
1104478570104478571GA23GENICpossibly homozygous971585620
1104478785104478786AG22GENIChomozygous971585621
1104478921104478922TC27GENIChomozygous971585622
1104479048104479049GC31GENICpossibly homozygous971585623
1104479358104479359TC31GENIChomozygous971585624
1104479677104479678CT34GENIChomozygous971585625
1104480400104480401GA21GENIChomozygous971585626
1104480826104480827AC18GENICpossibly homozygous971585627
1104480929104480930AG27GENIChomozygous971585628
1104481234104481235AG20GENIChomozygous971585629