chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
731169183116919GA19GENIChomozygous54619642
731182743118275GC22GENIChomozygous53768143
731185373118538TC16GENIChomozygous54619644
731188003118801TC12GENIChomozygous53768147
731190223119023CT8GENIChomozygous54619647
731191383119139GA11GENIChomozygous54165965
731191743119175GA15GENIChomozygous54619649
731191823119183T-16GENIChomozygous54165966
731194243119425TC14GENIChomozygous54619651
731195843119588CTTC----7GENIChomozygous54619653
731212683121269CG11GENIChomozygous54165970
731213393121340CT17GENIChomozygous54619661
731213403121341AG17GENIChomozygous54619663
731214273121428GC17GENIChomozygous53768159
731215443121545GA20GENIChomozygous53768161
731189773118978CCGTGTGTGT3GENIChomozygous56371756
731216793121680AC12GENIChomozygous54165974
731221563122157GC21GENIChomozygous54165975
731230603123061AT27GENIChomozygous54165976
731238623123863GGTT10GENIChomozygous54165979
731247313124732CCT11GENIChomozygous54165981
731250813125082GT18GENIChomozygous54165982
731253053125315GCCTGCCTCT----------21GENIChomozygous54165983
731255643125565A-13GENIChomozygous54165984
731269873126988A-9GENIChomozygous54165987
731281113128112GA13GENIChomozygous54165988
731286563128657CG14GENIChomozygous53768193
731309983130999CCGG11GENIChomozygous54165990
731366183136619CT13GENIChomozygous53768208
731377333137734CG13GENIChomozygous54165992
731401113140112TC18GENIChomozygous53768220
731417443141745GT7GENIChomozygous54165993