chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160374035160374036CG27GENIChomozygous114074134
5160374737160374738AT22GENIChomozygous114074135
5160375595160375596TC25GENIChomozygous114074137
5160375688160375689CT15GENIChomozygous114074138
5160375704160375705GA15GENIChomozygous114074139
5160375995160375996TA19GENIChomozygous114074140
5160376076160376077TC12GENIChomozygous114074141
5160376188160376189CT14GENIChomozygous114074142
5160376548160376549TC20GENIChomozygous114074143
5160376681160376682AC21GENIChomozygous114074144
5160377062160377063CT23GENIChomozygous114074145
5160378129160378130AT25GENIChomozygous114074146
5160378233160378234CT27GENIChomozygous114074148
5160378690160378691CT18GENIChomozygous114074149
5160378691160378692GT18GENIChomozygous114074150
5160378998160378999AG23GENIChomozygous114074151
5160379260160379261TC39GENIChomozygous114074152
5160379267160379268TC37GENIChomozygous114074153
5160379274160379275AG36GENIChomozygous114074154
5160379789160379790GA30GENIChomozygous114074155
5160380048160380049GA35GENIChomozygous118847342
5160380190160380191AG40GENIChomozygous114074156
5160380505160380506TC28GENIChomozygous114074157
5160380722160380723GC32GENIChomozygous114074158
5160381401160381402GA32GENIChomozygous114074159
5160381437160381438TC28GENIChomozygous114074160
5160381576160381577GA26GENIChomozygous114074161
5160383001160383002CT35GENIChomozygous114074162
5160383368160383369GA23GENIChomozygous114074163