chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6104623432104623433CT21GENIChomozygous114932133
6104623805104623806AG18GENIChomozygous114932134
6104626093104626094GA14GENIChomozygous114932138
6104626396104626397CA14GENIChomozygous114932139
6104626444104626445GA15GENIChomozygous118733182
6104626694104626695GA8GENICheterozygous118733183
6104627153104627154GT22GENIChomozygous114932142
6104627181104627182TG23GENIChomozygous114932143
6104627514104627515GC13GENIChomozygous114932145
6104627519104627520AG12GENICheterozygous114932146
6104627558104627559CT18GENIChomozygous114932147
6104627599104627600CT19GENIChomozygous118733184
6104628005104628006CT6GENIChomozygous118733185
6104629531104629532CG12GENIChomozygous114932154
6104629621104629622CA7GENIChomozygous118733186
6104629720104629721GA19GENIChomozygous118733187
6104629802104629803GA19GENIChomozygous118733188