chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226547015226547016CT19GENIChomozygous108558762
1226547617226547618GT24GENIChomozygous108558763
1226549466226549467AG23GENIChomozygous108558764
1226551006226551007CT18GENIChomozygous108558765
1226554865226554866GA24GENIChomozygous108558766
1226555171226555172CT17GENIChomozygous108558767
1226561625226561626GA16GENICheterozygous108558770
1226562503226562504AG18GENIChomozygous108558771
1226567558226567559TC13GENIChomozygous108558775
1226569051226569052AG10GENIChomozygous108558776
1226569745226569746GC24GENIChomozygous108558777
1226570086226570087AC12GENIChomozygous108558778
1226570728226570729GA19GENIChomozygous108558779
1226570850226570851TC8GENICheterozygous108558780
1226572164226572165TA7GENIChomozygous108558781