chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1259601981259601982CA25GENIChomozygous125493909
1259602143259602144GA15GENIChomozygous125493910
1259602168259602169CT21GENIChomozygous125493911
1259602204259602205CT31GENIChomozygous125493912
1259602229259602230AG25GENIChomozygous125493913
1259602931259602932CA18GENIChomozygous125493914
1259604061259604062AG6GENIChomozygous125493915
1259604538259604539TC13GENIChomozygous125323670
1259605025259605026GA8GENIChomozygous125493916
1259605711259605712CG21GENIChomozygous125493917
1259605921259605922AC7GENIChomozygous125493918
1259606380259606381CT22GENIChomozygous125493919
1259606535259606536GA6GENIChomozygous125493920
1259606999259607000AG18GENIChomozygous125493921
1259607212259607213CT15GENIChomozygous125493922
1259607390259607391GA12GENIChomozygous125493923
1259607454259607455AG18GENIChomozygous125493924
1259607517259607518GA9GENIChomozygous125493925
1259607651259607652CT10GENIChomozygous125442765
1259607813259607814AC12GENIChomozygous125493926
1259608049259608050GA20GENIChomozygous125493927
1259608117259608118AG22GENIChomozygous125323673
1259608373259608374GA23GENIChomozygous125493928