chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226547015226547016CT14GENIChomozygous108558762
1226547617226547618GT12GENIChomozygous108558763
1226549466226549467AG11GENIChomozygous108558764
1226551006226551007CT13GENIChomozygous108558765
1226554793226554794TC4GENICheterozygous125469278
1226554865226554866GA15GENIChomozygous108558766
1226555171226555172CT19GENIChomozygous108558767
1226561625226561626GA14GENIChomozygous108558770
1226562503226562504AG18GENIChomozygous108558771
1226567558226567559TC9GENIChomozygous108558775
1226569745226569746GC23GENIChomozygous108558777
1226570086226570087AC7GENIChomozygous108558778
1226570728226570729GA15GENIChomozygous108558779
1226570850226570851TC8GENIChomozygous108558780
1226572164226572165TA20GENIChomozygous108558781