chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5173341068173341069CT26GENIChomozygous785360131
5173342937173342938GC15GENIChomozygous785360132
5173344718173344719CT30GENIChomozygous785360133
5173345388173345389GA20GENIChomozygous785360134
5173345461173345462GA17GENIChomozygous785360135
5173345467173345468GA15GENIChomozygous785360136
5173345503173345504CT19GENIChomozygous785360137
5173347147173347148AG28GENIChomozygous785360138
5173347178173347179TC22GENIChomozygous785360139
5173347309173347310TA31GENIChomozygous785360140
5173347489173347490TC26GENIChomozygous785360141
5173347683173347684AG24GENIChomozygous785360142
5173348062173348063GT28GENIChomozygous785360143
5173348303173348304GA30GENICpossibly homozygous785360144
5173348372173348373AG32GENIChomozygous785360145
5173348932173348933GA17GENIChomozygous785360146
5173349421173349422TA19GENIChomozygous785360147
5173349703173349704AG18GENIChomozygous785360148
5173349906173349907AC15GENIChomozygous785360149
5173350381173350382TC19GENIChomozygous785360150
5173350440173350441GA25GENIChomozygous785360151
5173352655173352656CT20GENIChomozygous785360152
5173352692173352693AG22GENIChomozygous785360153
5173352901173352902TC29GENIChomozygous785360154
5173354070173354071GA23GENIChomozygous785360155