chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77029260570292606GA12GENIChomozygous116190114
77029339970293400AG13GENIChomozygous116190116
77029524470295245CA14GENIChomozygous116190118
77029536670295367TC17GENIChomozygous116190121
77029575170295752AG18GENIChomozygous116190123
77029587970295880GA14GENIChomozygous116190125
77029594370295944AG8GENIChomozygous116190127
77029781370297814TC18GENIChomozygous116190131
77029787970297880CT21GENIChomozygous116190133
77029992870299929AG13GENIChomozygous116190135
77030010370300104TC20GENIChomozygous116190137
77030098870300989CT13GENIChomozygous116190139
77030113770301138CT12GENIChomozygous116190141
77030150070301501GA21GENIChomozygous116190143
77030151570301516AG23GENIChomozygous116190145
77030207970302080TC14GENIChomozygous116190147
77030230070302301TA12GENIChomozygous116190149
77030310570303106CT21GENIChomozygous116190151
77030355670303557GA25GENIChomozygous116190153
77030373570303736TC14GENIChomozygous116190155
77030436570304366CT7GENIChomozygous116190157
77030461570304616TC18GENIChomozygous115708831
77030528370305284AG18GENIChomozygous116190159
77030576470305765CA31GENIChomozygous116190161
77030579370305794TC20GENIChomozygous116190163
77030678270306783GA27GENIChomozygous116190165
77030870870308709CT17GENIChomozygous115708834
77030900270309003CT6GENIChomozygous116190167
77030978570309786CT19GENIChomozygous116190169