chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187011438670114387CT45GENIChomozygous46747055
187011457170114572AT20GENIChomozygous46627116
187011482270114823AT8GENICheterozygous46747056
187011501770115018TC25GENIChomozygous46627117
187011502370115024CT23GENIChomozygous46627118
187011516370115164GGT3GENIChomozygous46627119
187011521470115215GGT15GENIChomozygous46747057
187011654470116545GC16GENIChomozygous46627123
187011773870117739GGA20GENIChomozygous46627125
187011808470118085T-16GENIChomozygous46627126
187011812970118141TTTCTTTCTTTC------------4GENIChomozygous46747058
187011843870118439T-1GENIChomozygous46747059
187011878670118787TTTTC3GENICheterozygous46627128
187011878670118787TTTC3GENICheterozygous46627129
187011885370118854CT28GENICpossibly homozygous46627131
187011899670118997GT33GENICpossibly homozygous46627132
187011899870118999GT31GENICpossibly homozygous46627133
187011901870119019GT25GENICpossibly homozygous46627134
187011909370119094AG13GENICpossibly homozygous46627135
187011935570119358GGG---17GENIChomozygous46747060
187011948170119482CA20GENIChomozygous46627139
187011954670119547GGT16GENIChomozygous46507264
187011966570119666CG41GENIChomozygous46627140
187011978570119786AG50GENICheterozygous46627141
187011979570119796GA48GENICheterozygous46627142
187011994170119942CT20GENIChomozygous46627144
187011994970119950G-15GENIChomozygous46627145
187012002870120029GC12GENIChomozygous46627146
187012021470120215GA6GENIChomozygous46627147
187012039970120400AG17GENIChomozygous46627148
187012055970120560C-7GENIChomozygous46507265
187012055970120560CCCT9GENIChomozygous46507267
187012115470121155GA29GENIChomozygous46627150
187012131270121313CT33GENIChomozygous46627151
187012168870121693TGACA-----29GENIChomozygous46627152
187012195270121953GA21GENIChomozygous46627153
187012245370122454CT38GENIChomozygous46627154
187012252870122529AG42GENIChomozygous46627155