chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160374035160374036CG21GENIChomozygous114074134
5160374737160374738AT25GENIChomozygous114074135
5160375033160375034GA17GENIChomozygous114074136
5160375595160375596TC27GENIChomozygous114074137
5160375688160375689CT19GENIChomozygous114074138
5160375704160375705GA22GENIChomozygous114074139
5160375995160375996TA18GENIChomozygous114074140
5160376076160376077TC10GENIChomozygous114074141
5160376188160376189CT9GENIChomozygous114074142
5160376548160376549TC8GENIChomozygous114074143
5160377062160377063CT17GENIChomozygous114074145
5160377491160377492AC11GENIChomozygous118937414
5160378129160378130AT16GENIChomozygous114074146
5160378197160378198CG17GENIChomozygous114074147
5160378201160378202CG16GENIChomozygous114259560
5160378690160378691CT19GENIChomozygous114074149
5160378691160378692GT18GENIChomozygous114074150
5160378998160378999AG14GENIChomozygous114074151
5160379260160379261TC22GENIChomozygous114074152
5160379267160379268TC23GENIChomozygous114074153
5160379274160379275AG25GENIChomozygous114074154
5160379789160379790GA20GENIChomozygous114074155
5160380048160380049GA15GENIChomozygous118847342
5160380190160380191AG28GENIChomozygous114074156
5160380505160380506TC6GENIChomozygous114074157
5160380722160380723GC17GENIChomozygous114074158
5160381401160381402GA13GENIChomozygous114074159
5160381437160381438TC11GENIChomozygous114074160
5160381576160381577GA15GENIChomozygous114074161
5160383001160383002CT17GENIChomozygous114074162
5160383368160383369GA14GENIChomozygous114074163