chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134944516749445168TC18GENIChomozygous191029153
134944548549445486TC28GENIChomozygous191029154
134944573349445734CT20GENIChomozygous191029155
134944578149445782AC23GENIChomozygous191029156
134944588849445889GA22GENIChomozygous191029157
134944615849446159GC10GENIChomozygous188353751
134944650949446510TA22GENIChomozygous191029158
134944652249446523GA17GENIChomozygous188353752
134944654849446549GC15GENIChomozygous188353753
134944697249446973GA19GENIChomozygous188353754
134944717449447175CT29GENIChomozygous188353755
134944723649447237AT30GENICpossibly homozygous191029159
134944740049447401TC17GENIChomozygous191029160