chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226545900226545901CT34GENIChomozygous120595694
1226547015226547016CT24GENIChomozygous108558762
1226547265226547266AT19GENICheterozygous120876545
1226549466226549467AG22GENIChomozygous108558764
1226551006226551007CT21GENIChomozygous108558765
1226554865226554866GA28GENIChomozygous108558766
1226555171226555172CT38GENIChomozygous108558767
1226557194226557195GA34GENICpossibly homozygous120876546
1226559484226559485TC30GENIChomozygous108558769
1226561625226561626GA23GENIChomozygous108558770
1226562503226562504AG30GENICpossibly homozygous108558771
1226565402226565403TA19GENICpossibly homozygous120595696
1226567558226567559TC28GENICpossibly homozygous108558775
1226569051226569052AG21GENIChomozygous108558776
1226570086226570087AC23GENICpossibly homozygous108558778
1226570728226570729GA36GENICpossibly homozygous108558779
1226570850226570851TC20GENICpossibly homozygous108558780