chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71248857112488572TC7GENIChomozygous53791066
71248865812488659TC10GENIChomozygous53791067
71248899612488997CT8GENIChomozygous53791069
71248935712489358GA10GENIChomozygous53791070
71248967212489673TC12GENIChomozygous53791071
71248967812489679C-13GENIChomozygous53791072
71248973112489732AAG15GENIChomozygous53791073
71248983612489837CG12GENIChomozygous53791074
71249072712490728TC3GENIChomozygous53791075
71249172812491729GA11GENIChomozygous56142273
71249202912492030A-6GENIChomozygous54630389
71249254112492542GA7GENICpossibly homozygous53791077
71249266212492663CT16GENIChomozygous53791078
71249307712493078TC18GENIChomozygous53791079
71249404012494041GC20GENIChomozygous56142276
71249430112494302T-21GENIChomozygous56142279