chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5146851882146851883AAT13GENIChomozygous55774070
5146852734146852735GGT2GENIChomozygous55774074
5146853232146853233A-12GENICpossibly homozygous56069827
5146853406146853407TC15GENIChomozygous55774078
5146853515146853516GA23GENICpossibly homozygous55774080
5146855740146855741GA19GENICpossibly homozygous55774082
5146856158146856159AC10GENIChomozygous55774088
5146859272146859273CT5GENIChomozygous55774093
5146859278146859279TC9GENIChomozygous55774095
5146859967146859968A-8GENICpossibly homozygous55774097
5146860034146860035GA18GENIChomozygous55774099
5146860248146860249TC17GENIChomozygous55774105
5146862027146862028G-7GENIChomozygous55774113
5146863669146863670CT35GENIChomozygous55774117
5146867365146867374CAGCTCTCA---------4GENIChomozygous55774123
5146867742146867743AAAAAC3GENIChomozygous55774125
5146869351146869352GA31GENICpossibly homozygous55774127
5146870175146870199TATGTATGTATGTATGTATGTATG------------------------4GENIChomozygous56355477