chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76365659163656592GT29GENIChomozygous115694590
76365663963656640TC19GENIChomozygous115694591
76365813263658133AG24GENIChomozygous115694592
76365860563658605AGAGGG23GENIChomozygous128471976
76365956663659567GA28GENIChomozygous115694593
76366039863660399AG34GENIChomozygous115694594
76366039963660400TG34GENIChomozygous115694595
76366065263660653GC26GENIChomozygous115694596
76366107663661077AG20GENIChomozygous115694597
76366235863662359TA39GENIChomozygous115694598
76366500263665003CT17GENIChomozygous115694599
76366540163665402TC19GENIChomozygous115694600
76366757663667577GA25GENIChomozygous115694601
76366812563668126TC17GENIChomozygous115694602
76366818163668182TC19GENIChomozygous115694603
76366920963669210C7GENIChomozygous128471977
76366954763669550GGT10GENIChomozygous128471978
76367026563670266CT23GENIChomozygous115694604
76367037763670378TC18GENIChomozygous115694605
76367038763670388TC16GENIChomozygous122787655
76367039263670393A17GENIChomozygous128471979
76367039463670395AT17GENIChomozygous122787657
76367189463671894TGG23GENIChomozygous128471980
76367235763672358CT32GENIChomozygous115694607
76367338963673390CT19GENIChomozygous115694608
76367403963674040GT12GENIChomozygous115694609
76367404263674042T12GENICheterozygous128471981
76367407863674079CT17GENICheterozygous115694610
76367583463675835GA26GENIChomozygous115694611
76367839563678396CT30GENIChomozygous115694612
76367854463678545TC41GENIChomozygous115694613
76367408963674090CT18GENICheterozygous128553622
76367038163670381CTT18GENIChomozygous132108459
76368475063684751AG23GENIChomozygous115694616
76368555363685554AG13GENIChomozygous115694617
76368605163686052TC28GENIChomozygous115694618
76368617263686175CTC15GENIChomozygous128471982
76368709463687095CT23GENIChomozygous115694619