chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1175844088175844088T43GENICpossibly homozygous130828031
1175844371175844378TGTACCC42GENIChomozygous130828032
1175848804175848804AAAT38GENIChomozygous127458432
1175849201175849205GTTA50GENIChomozygous127458433
1175850044175850050AAGAAA46GENIChomozygous130828033
1175850287175850288TC44GENIChomozygous108395133
1175850706175850707TC55GENIChomozygous108395135
1175853456175853460TATT37GENIChomozygous130828034
1175857476175857477AG52GENIChomozygous108962078
1175857597175857598AG58GENIChomozygous108395141
1175858575175858576CT48GENIChomozygous108962079
1175861140175861140TC42GENIChomozygous127458434
1175862559175862560TC56GENIChomozygous108395149
1175864702175864703CT59GENIChomozygous108962080
1175866822175866823AG39GENIChomozygous108395153
1175868356175868357GA55GENIChomozygous108962082