chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4176510009176510010TC18GENIChomozygous112963990
4176510250176510250G18GENIChomozygous128107904
4176510303176510304AG12GENIChomozygous112963992
4176510956176510957TC18GENIChomozygous112963994
4176511450176511454AAAT12GENIChomozygous128107905
4176512622176512623AT12GENIChomozygous112963996
4176513229176513237TCTATCTA13GENIChomozygous128107906
4176514517176514517C13GENIChomozygous128107907
4176514776176514777TA12GENICpossibly homozygous112964012
4176513335176513336GT17GENIChomozygous112963998
4176513369176513370AG18GENIChomozygous112964000
4176513809176513810AG15GENIChomozygous112964002
4176513899176513900TC16GENIChomozygous112964004
4176514199176514200AT9GENIChomozygous112964006
4176514642176514643AC14GENIChomozygous112964008
4176514745176514746GA14GENIChomozygous112964010
4176516152176516153G20GENIChomozygous128107908
4176517892176517893AG19GENIChomozygous112964014