chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76365659163656592GT15GENIChomozygous115694590
76365663963656640TC16GENIChomozygous115694591
76365813263658133AG13GENIChomozygous115694592
76365956663659567GA18GENIChomozygous115694593
76366039863660399AG17GENIChomozygous115694594
76366039963660400TG18GENIChomozygous115694595
76366065263660653GC9GENIChomozygous115694596
76366107663661077AG12GENIChomozygous115694597
76366235863662359TA15GENIChomozygous115694598
76366500263665003CT19GENIChomozygous115694599
76366540163665402TC26GENIChomozygous115694600
76366757663667577GA16GENIChomozygous115694601
76366812563668126TC16GENIChomozygous115694602
76366818163668182TC19GENIChomozygous115694603
76367026563670266CT19GENIChomozygous115694604
76367235763672358CT14GENIChomozygous115694607
76367338963673390CT20GENIChomozygous115694608
76367583463675835GA30GENIChomozygous115694611
76367839563678396CT20GENIChomozygous115694612
76367854463678545TC16GENIChomozygous115694613
76368475063684751AG21GENIChomozygous115694616
76368555363685554AG13GENIChomozygous115694617
76368605163686052TC12GENIChomozygous115694618
76368709463687095CT22GENIChomozygous115694619