chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81169377511693776CT46GENIChomozygous142035403
81169396811693969CT45GENIChomozygous142035404
81169430211694303TC41GENIChomozygous142035405
81169517211695176CACT11GENIChomozygous142017194
81169643611696437TC45GENIChomozygous142035406
81169644911696450GA44GENIChomozygous142035407
81169724311697245CA10GENICheterozygous142017195
81169839511698396GA46GENIChomozygous142035408
81169860511698606CT44GENIChomozygous142035409
81169896511698966AG34GENICpossibly homozygous142035410
81169957811699579TG47GENIChomozygous142035411
81169958211699583TC48GENIChomozygous142035412
81169971111699731CTTGGAACTTCTAGGAGGCA24GENIChomozygous142017196
81169976411699765GA31GENIChomozygous142035413
81170026611700267TC39GENIChomozygous142035414
81170060211700602CACT32GENIChomozygous142017197
81170078211700783GC35GENIChomozygous142035415
81170103111701032GA35GENIChomozygous142035416
81170143211701433TC55GENIChomozygous142035417
81170170811701709CT47GENIChomozygous142035418
81170242611702427CT46GENIChomozygous142035419
81170308211703083TA51GENIChomozygous142035420
81170313411703135TA37GENIChomozygous142035421
81170321911703220TC46GENIChomozygous142035422