chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160374737160374738AT27GENIChomozygous114074135
5160375033160375034GA35GENIChomozygous114074136
5160375071160375072CT31GENIChomozygous114359190
5160375595160375596TC24GENIChomozygous114074137
5160375688160375689CT18GENIChomozygous114074138
5160375704160375705GA19GENIChomozygous114074139
5160376076160376077TC38GENIChomozygous114074141
5160376188160376189CT20GENIChomozygous114074142
5160376548160376549TC30GENIChomozygous114074143
5160376681160376682AC28GENIChomozygous114074144
5160377062160377063CT28GENIChomozygous114074145
5160378129160378130AT28GENIChomozygous114074146
5160378189160378190CG30GENICheterozygous114259556
5160378193160378194CG30GENICheterozygous114259558
5160378197160378198CG30GENICheterozygous114074147
5160378233160378234CT23GENIChomozygous114074148
5160378998160378999AG31GENIChomozygous114074151
5160379260160379261TC42GENIChomozygous114074152
5160379267160379268TC35GENIChomozygous114074153
5160379274160379275AG36GENIChomozygous114074154
5160379789160379790GA23GENIChomozygous114074155
5160380054160380055GA22GENICpossibly homozygous114359192
5160380190160380191AG18GENIChomozygous114074156
5160380505160380506TC17GENIChomozygous114074157
5160381437160381438TC46GENIChomozygous114074160
5160380722160380723GC29GENIChomozygous114074158
5160381401160381402GA32GENIChomozygous114074159
5160381576160381577GA24GENIChomozygous114074161
5160382952160382953AT31GENIChomozygous114359194
5160383001160383002CT29GENIChomozygous114074162
5160383056160383057GA29GENIChomozygous114359196
5160383368160383369GA36GENIChomozygous114074163