chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187011438670114387CT10GENIChomozygous46747055
187011457170114572AT16GENIChomozygous46627116
187011482270114823AT18GENIChomozygous46747056
187011501770115018TC23GENIChomozygous46627117
187011502370115024CT24GENIChomozygous46627118
187011516370115164GGT10GENIChomozygous46627119
187011521470115215GGT10GENIChomozygous46747057
187011654470116545GC20GENIChomozygous46627123
187011656070116561A-14GENICheterozygous46987257
187011773870117739GGA28GENIChomozygous46627125
187011808470118085T-19GENIChomozygous46627126
187011812970118141TTTCTTTCTTTC------------6GENIChomozygous46747058
187011885370118854CT8GENIChomozygous46627131
187011899670118997GT9GENIChomozygous46627132
187011899870118999GT8GENIChomozygous46627133
187011935570119358GGG---7GENIChomozygous46747060
187011948170119482CA11GENIChomozygous46627139
187011966570119666CG20GENICpossibly homozygous46627140
187012002870120029GC28GENICpossibly homozygous46627146
187012021470120215GA13GENIChomozygous46627147
187012039970120400AG7GENIChomozygous46627148
187012115470121155GA12GENIChomozygous46627150
187012131270121313CT11GENIChomozygous46627151
187012168870121693TGACA-----11GENIChomozygous46627152
187012195270121953GA20GENIChomozygous46627153
187012245370122454CT16GENIChomozygous46627154
187012252870122529AG20GENIChomozygous46627155
187011954670119547GGT13GENIChomozygous46507264