chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76365659163656592GT24GENIChomozygous115694590
76365663963656640TC18GENIChomozygous115694591
76365813263658133AG22GENIChomozygous115694592
76365860563658605AGAGGG20GENIChomozygous128471976
76365956663659567GA10GENIChomozygous115694593
76366039863660399AG22GENIChomozygous115694594
76366039963660400TG22GENIChomozygous115694595
76366065263660653GC10GENIChomozygous115694596
76366107663661077AG11GENIChomozygous115694597
76366235863662359TA19GENIChomozygous115694598
76366500263665003CT14GENIChomozygous115694599
76366540163665402TC18GENIChomozygous115694600
76366757663667577GA30GENIChomozygous115694601
76366812563668126TC27GENIChomozygous115694602
76366818163668182TC24GENIChomozygous115694603
76366920963669210C4GENIChomozygous128471977
76366954763669550GGT15GENIChomozygous128471978
76367026563670266CT30GENIChomozygous115694604
76367037763670378TC18GENIChomozygous115694605
76367038763670388TC17GENIChomozygous122787655
76367039263670393A17GENIChomozygous128471979
76367039463670395AT17GENIChomozygous122787657
76367189463671894TGG20GENIChomozygous128471980
76367235763672358CT21GENIChomozygous115694607
76367338963673390CT11GENIChomozygous115694608
76367403963674040GT5GENIChomozygous115694609
76367407863674079CT5GENICheterozygous115694610
76367583463675835GA18GENIChomozygous115694611
76367839563678396CT26GENIChomozygous115694612
76367854463678545TC23GENIChomozygous115694613
76368475063684751AG29GENIChomozygous115694616
76368555363685554AG17GENIChomozygous115694617
76368605163686052TC23GENIChomozygous115694618
76368617263686175CTC15GENIChomozygous128471982
76368709463687095CT22GENIChomozygous115694619