chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76365659163656592GT67GENICpossibly homozygous115694590
76365663963656640TC56GENIChomozygous115694591
76365813263658133AG47GENIChomozygous115694592
76365860563658605AGAGGG45GENIChomozygous128471976
76365956663659567GA44GENIChomozygous115694593
76366039863660399AG50GENIChomozygous115694594
76366039963660400TG51GENIChomozygous115694595
76366065263660653GC62GENIChomozygous115694596
76366107663661077AG60GENIChomozygous115694597
76366235863662359TA50GENIChomozygous115694598
76366500263665003CT34GENIChomozygous115694599
76366540163665402TC37GENIChomozygous115694600
76366757663667577GA66GENIChomozygous115694601
76366812563668126TC46GENIChomozygous115694602
76366818163668182TC43GENIChomozygous115694603
76366920963669210C8GENIChomozygous128471977
76366954763669550GGT43GENIChomozygous128471978
76367026563670266CT57GENIChomozygous115694604
76367037763670378TC40GENIChomozygous115694605
76367038763670388TC41GENIChomozygous122787655
76367039263670393A39GENIChomozygous128471979
76367039463670395AT39GENIChomozygous122787657
76367189463671894TGG41GENIChomozygous128471980
76367235763672358CT52GENIChomozygous115694607
76367338963673390CT53GENIChomozygous115694608
76367403963674040GT30GENIChomozygous115694609
76367404263674042T26GENICheterozygous128471981
76367407863674079CT29GENICheterozygous115694610
76367408963674090CT32GENICheterozygous128553622
76367583463675835GA31GENIChomozygous115694611
76367839563678396CT67GENIChomozygous115694612
76367854463678545TC64GENIChomozygous115694613
76368475063684751AG55GENIChomozygous115694616
76368555363685554AG52GENIChomozygous115694617
76368605163686052TC52GENIChomozygous115694618
76368617263686175CTC59GENIChomozygous128471982
76368709463687095CT53GENIChomozygous115694619