chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129798708129798709CT7GENIChomozygous1000764849
7129799658129799659GA5GENIChomozygous1000764850
7129800613129800614CT11GENIChomozygous1000764851
7129801117129801118AG10GENIChomozygous1000764852
7129801936129801937GA5GENIChomozygous1000764853
7129804694129804695TG8GENIChomozygous1000764854
7129804776129804777TC6GENIChomozygous1000764855
7129804821129804822GA2GENIChomozygous1000764856
7129805161129805162TC5GENIChomozygous1000764857
7129805282129805283AG11GENIChomozygous1000764858
7129805315129805316TC11GENIChomozygous1000764859
7129805327129805328GT10GENIChomozygous1000764860
7129806589129806590CT5GENIChomozygous1000764861
7129807636129807637CA3GENIChomozygous1000764862
7129808777129808778CT6GENIChomozygous1000764863
7129808911129808912GT8GENIChomozygous1000764864
7129808987129808988AG11GENIChomozygous1000764865
7129810320129810321TC8GENIChomozygous1000764866
7129810349129810350TC11GENIChomozygous1000764867
7129810795129810796CT6GENIChomozygous1000764868
7129810829129810830GA10GENIChomozygous1000764869
7129811223129811224AG2GENIChomozygous1000764870