chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187011438670114387CT4GENIChomozygous46747055
187011457170114572AT5GENIChomozygous46627116
187011482270114823AT7GENIChomozygous46747056
187011501770115018TC4GENIChomozygous46627117
187011502370115024CT3GENIChomozygous46627118
187011516370115164GGT7GENICheterozygous46627119
187011521470115215GGT11GENIChomozygous46747057
187011625370116254CCTGATTTTTTCTTTTAAATCAAAGGTACGT4GENIChomozygous46821635
187011654470116545GC7GENIChomozygous46627123
187011773870117739GGA3GENIChomozygous46627125
187011808470118085T-11GENIChomozygous46627126
187011812970118141TTTCTTTCTTTC------------9GENIChomozygous46747058
187011843870118439T-7GENIChomozygous46747059
187011878670118787TTTC4GENIChomozygous46627129
187011885370118854CT2GENIChomozygous46627131
187011899670118997GT2GENIChomozygous46627132
187011899870118999GT2GENIChomozygous46627133
187011901870119019GT3GENIChomozygous46627134
187011935570119358GGG---7GENIChomozygous46747060
187011948170119482CA12GENIChomozygous46627139
187011954670119547GGT9GENIChomozygous46507264
187011966570119666CG6GENIChomozygous46627140
187011978570119786AG7GENIChomozygous46627141
187011979570119796GA5GENIChomozygous46627142
187011994170119942CT3GENIChomozygous46627144
187011994970119950G-4GENIChomozygous46627145
187011997770119979CG--6GENIChomozygous46800059
187011995070119951GA5GENIChomozygous46800055
187011997370119974GGCT7GENIChomozygous46800057
187012002870120029GC6GENIChomozygous46627146
187012021470120215GA5GENIChomozygous46627147
187012039970120400AG5GENIChomozygous46627148
187012055970120560CCCTCCTCCTCCT2GENIChomozygous46821636
187012115470121155GA8GENIChomozygous46627150
187012131270121313CT7GENIChomozygous46627151
187012168870121693TGACA-----5GENIChomozygous46627152
187012195270121953GA7GENIChomozygous46627153
187012245370122454CT6GENIChomozygous46627154
187012252870122529AG11GENIChomozygous46627155