chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160374737160374738AT31GENIChomozygous114074135
5160375033160375034GA35GENIChomozygous114074136
5160375595160375596TC32GENIChomozygous114074137
5160375688160375689CT24GENIChomozygous114074138
5160375704160375705GA21GENIChomozygous114074139
5160376076160376077TC43GENIChomozygous114074141
5160376188160376189CT39GENIChomozygous114074142
5160376548160376549TC44GENIChomozygous114074143
5160376681160376682AC34GENIChomozygous114074144
5160376856160376857GC39GENIChomozygous114160888
5160377062160377063CT28GENIChomozygous114074145
5160378129160378130AT48GENIChomozygous114074146
5160378205160378206CG37GENICheterozygous114544837
5160378233160378234CT41GENIChomozygous114074148
5160378998160378999AG50GENIChomozygous114074151
5160379260160379261TC43GENIChomozygous114074152
5160379267160379268TC44GENIChomozygous114074153
5160379274160379275AG43GENIChomozygous114074154
5160379789160379790GA24GENIChomozygous114074155
5160380190160380191AG13GENIChomozygous114074156
5160380471160380472GC20GENICheterozygous114160889
5160380505160380506TC19GENIChomozygous114074157
5160380722160380723GC34GENIChomozygous114074158
5160381401160381402GA42GENIChomozygous114074159
5160381437160381438TC38GENIChomozygous114074160
5160381576160381577GA34GENIChomozygous114074161
5160381784160381785CA34GENICpossibly homozygous114160890
5160383001160383002CT31GENIChomozygous114074162
5160383368160383369GA18GENIChomozygous114074163