chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
195850719158507192TG21GENICpossibly homozygous109792750
195850762058507621AG23GENIChomozygous109745137
195850776858507769AC29GENICpossibly homozygous109792752
195850780158507802GT18GENIChomozygous109826112
195850829358508294GC42GENIChomozygous109745141
195850838458508385GA37GENIChomozygous109792754
195850841558508416CA30GENIChomozygous109745143
195850848158508482GA19GENIChomozygous109745145
195850849358508494CT25GENICpossibly homozygous109792756
195850850758508508GA26GENIChomozygous109745147
195850855658508557CA22GENIChomozygous109745149