chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181553418615534187TTC4GENIChomozygous46367886
181553422415534225GT21GENIChomozygous46575354
181553601315536014AG18GENIChomozygous46682511
181553640315536404TTG11GENIChomozygous46575355
181553640415536405GGGA11GENIChomozygous46575356
181554170515541706CT22GENIChomozygous46575357
181554194315541944AG38GENICpossibly homozygous46367889
181554203515542036AG40GENIChomozygous46575358