chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106582361165823612TC24GENIChomozygous51907207
106582418265824183GA20GENIChomozygous51478384
106582558765825588TC23GENIChomozygous51478387
106582604165826042GC12GENIChomozygous51478389
106582646465826465GGTGA16GENIChomozygous51478391
106582671065826711AATT7GENICpossibly homozygous51478393
106582762565827626TC20GENICpossibly homozygous51478394
106582792765827929AA--21GENIChomozygous51478395
106582820265828204TT--10GENIChomozygous51907211
106582897665828977TC16GENIChomozygous51478398
106582903465829041ATTGTGG-------11GENIChomozygous51907213
106582912465829125TC18GENIChomozygous51907215
106582974565829746GA18GENICpossibly homozygous51478400
106582980365829804GGCCTAGCAAGCGCAAGGC12GENIChomozygous51478401
106583049265830493GC20GENIChomozygous51478402
106583115765831158TC20GENIChomozygous51478403
106583125765831258CT22GENIChomozygous51907217
106583170865831709TC30GENIChomozygous51478404
106583203665832037TG32GENIChomozygous51478405
106583207165832072G-30GENIChomozygous51478406