chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3105056451105056452GA41GENIChomozygous141523814
3105057191105057192GC7GENICheterozygous403072618
3105057191105057192G7GENIChomozygous403072619
3105058084105058085TC52GENIChomozygous136781569
3105058709105058710TC39GENIChomozygous136781572
3105059215105059216AC40GENIChomozygous136781573
3105060900105060901G23GENICpossibly homozygous403072620
3105060900105060901GA23GENICheterozygous403072621
3105060904105060905G23GENICpossibly homozygous403072622
3105060904105060905GA23GENICheterozygous403072623
3105060908105060909G23GENICpossibly homozygous403072624
3105060908105060909GA23GENICheterozygous403072625
3105061188105061189GT32GENIChomozygous136781574
3105061365105061366TC35GENIChomozygous141523815
3105061390105061391GC40GENIChomozygous136781575
3105061391105061392CT40GENIChomozygous136781576
3105061476105061477CA38GENIChomozygous136781577
3105062496105062497AG32GENIChomozygous136781578
3105063132105063133AT56GENIChomozygous136781579
3105063499105063500GC40GENIChomozygous136781580
3105063548105063549AG35GENIChomozygous136781581
3105063575105063576GC38GENIChomozygous136781582
3105063590105063591AT43GENIChomozygous136781583
3105064114105064115GT39GENIChomozygous136781584
3105065006105065007TC54GENIChomozygous136781585
3105065328105065329AG55GENIChomozygous136781586
3105065696105065697AT48GENIChomozygous136781587
3105067227105067228AG42GENIChomozygous136781589
3105067592105067593CA35GENIChomozygous136781590
3105067994105067995CT47GENIChomozygous141523816
3105067998105067999GA46GENIChomozygous136781591
3105068497105068498GA27GENICpossibly homozygous136781592
3105070637105070638CA40GENIChomozygous141523817
3105068560105068560CTT16GENICheterozygous144630489
3105067220105067220TTGAC45GENIChomozygous136581542
3105063114105063126CAGAAAGCAAAC57GENIChomozygous136581541
3105061009105061013CACA35GENIChomozygous136581540
3105068561105068561T16GENICheterozygous136581543