chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113088025530880256CT34GENICheterozygous804185416
113088065030880651AG37GENIChomozygous804185417
113088115030881151CT33GENIChomozygous804185418
113088138830881389TC15GENIChomozygous804185419
113088321630883217TC25GENIChomozygous804185420
113088331430883315GC24GENIChomozygous804185421
113088373230883733TG29GENIChomozygous804185422
113088448630884487AG24GENIChomozygous804185423
113088583130885832CT27GENIChomozygous804185424
113088615730886158CT27GENIChomozygous804185425
113088679530886796TC13GENIChomozygous804185426
113088717930887180TC30GENIChomozygous804185427
113088725730887258GA25GENICpossibly homozygous804185428
113088948030889481AG35GENIChomozygous804185429
113088960030889601CT31GENIChomozygous804185430
113088998630889987AG21GENIChomozygous804185431
113089008130890082TG12GENIChomozygous804185432
113089283830892839TC29GENIChomozygous804185433