chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16437636564376366TA5GENIChomozygous120897607
16437638064376381GT6GENIChomozygous109095022
16437671864376719TC6GENIChomozygous109095024
16437776364377764GA5GENIChomozygous120897608
16437897564378976AG3GENIChomozygous120897609
16437905264379053AG7GENIChomozygous109095028
16437918764379188TC9GENIChomozygous109095030
16437962264379623GA7GENIChomozygous120897610
16438654664386547CT6GENIChomozygous120897611
16438655264386553GA6GENIChomozygous109287567
16438819264388193AG5GENIChomozygous109095058
16438906264389063GT12GENIChomozygous109095060
16438919664389197GA5GENIChomozygous120897612
16438962164389622TC10GENIChomozygous109095066
16439018864390189AT6GENIChomozygous120897613
16439154064391541CT10GENIChomozygous109095072
16439190264391903GA8GENIChomozygous120897614
16439346164393462CT8GENIChomozygous120897615
16439393864393939GA6GENIChomozygous120897616
16439400964394010AC11GENIChomozygous109095078
16439673864396739TC4GENIChomozygous109095090
16439725564397256AG6GENIChomozygous109095092
16439795464397955AG5GENIChomozygous109095094
16439882664398827CA6GENIChomozygous120897617
16439974764399748GA11GENIChomozygous120897618
16440015964400160TG2GENIChomozygous109095104
16440325264403253TG14GENIChomozygous109095106
16440401464404015AG2GENIChomozygous109095112
16440449064404491TC4GENIChomozygous109095114
16440499664404997GA4GENIChomozygous109095118