chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76365659163656592GT23GENIChomozygous115694590
76365663963656640TC15GENICpossibly homozygous115694591
76365813263658133AG16GENIChomozygous115694592
76365860563658605AGAGGG13GENIChomozygous128471976
76365956663659567GA17GENIChomozygous115694593
76366039863660399AG18GENIChomozygous115694594
76366039963660400TG18GENIChomozygous115694595
76366065263660653GC19GENIChomozygous115694596
76366107663661077AG22GENIChomozygous115694597
76366235863662359TA9GENIChomozygous115694598
76366457063664571CT17GENIChomozygous118412397
76366500263665003CT17GENIChomozygous115694599
76366540163665402TC26GENIChomozygous115694600
76366757663667577GA14GENIChomozygous115694601
76366812563668126TC17GENIChomozygous115694602
76366818163668182TC17GENIChomozygous115694603
76366911563669116GT20GENICheterozygous130565456
76366920963669210C8GENIChomozygous128471977
76366954763669550GGT11GENIChomozygous128471978
76367026563670266CT19GENIChomozygous115694604
76367037763670378TC23GENIChomozygous115694605
76367038763670388TC23GENIChomozygous122787655
76367039263670393A22GENIChomozygous128471979
76367189463671894TGG19GENIChomozygous128471980
76367403963674040GT14GENIChomozygous115694609
76367039463670395AT23GENIChomozygous122787657
76367235763672358CT15GENIChomozygous115694607
76367338963673390CT23GENIChomozygous115694608
76367404263674042T12GENICheterozygous128471981
76367407863674079CT8GENICheterozygous115694610
76367408963674090CT7GENICheterozygous128553622
76368475063684751AG16GENIChomozygous115694616
76367583463675835GA15GENIChomozygous115694611
76367839563678396CT21GENIChomozygous115694612
76367854463678545TC17GENIChomozygous115694613
76368555363685554AG23GENIChomozygous115694617
76368605163686052TC15GENIChomozygous115694618
76368617263686175CTC11GENIChomozygous128471982
76368709463687095CT26GENIChomozygous115694619