chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3164173067164173068CT11GENIChomozygous111806827
3164176508164176509CT15GENIChomozygous111806831
3164176919164176920TC15GENIChomozygous111806833
3164177585164177586TC9GENIChomozygous111806835
3164177707164177708CT13GENIChomozygous111806837
3164177851164177852TC15GENIChomozygous111806839
3164178674164178675AG10GENIChomozygous111806841
3164180257164180258CT9GENICheterozygous111806845
3164180828164180829CT10GENIChomozygous111806847
3164181745164181746GA16GENIChomozygous111806849
3164182663164182664TA10GENIChomozygous111806851
3164183040164183041CT26GENICpossibly homozygous111806853
3164183259164183260GA12GENIChomozygous111806855
3164189864164189865CT11GENIChomozygous111806867
3164191492164191493GT25GENICheterozygous111806869
3164194526164194527CT9GENIChomozygous111806873
3164195280164195281CT10GENIChomozygous111806875
3164195759164195760CT5GENIChomozygous111806877
3164197859164197860AG15GENIChomozygous111806879
3164198567164198568GA14GENIChomozygous111806881
3164202116164202117GA12GENIChomozygous111806883
3164203012164203013TG23GENIChomozygous111806885
3164203266164203267TC20GENIChomozygous111806887
3164204176164204177AG16GENIChomozygous111806891
3164205290164205291TC18GENIChomozygous111806893
3164208321164208322AG18GENIChomozygous111806897
3164210253164210254TC5GENICheterozygous125916809
3164215500164215501GA17GENIChomozygous111806907
3164217527164217528GC17GENIChomozygous111806909
3164219444164219445GA4GENIChomozygous111806911
3164220288164220289AG15GENICheterozygous111806915
3164222180164222181CT16GENIChomozygous111806917
3164222369164222370AG7GENIChomozygous111806919