chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86047139760471398GA46GENIChomozygous52984639
86047144560471446AAT39GENIChomozygous52984640
86047144860471451TGT---38GENIChomozygous52984642
86047179060471791GA48GENIChomozygous52984644
86047217060472171CT71GENIChomozygous52984645
86047331160473312AG60GENIChomozygous52984647
86047332560473326GA65GENICpossibly homozygous52984648
86047378660473787GA50GENICpossibly homozygous52984650
86047380260473803GA52GENICpossibly homozygous52984651
86047417360474174GGAAAA45GENIChomozygous52984653
86047739960477400CG17GENIChomozygous52666508
86047740260477403T-16GENIChomozygous52666510
86047780060477801CCT1GENIChomozygous52666514
86047780560477806GC4GENIChomozygous52666516
86047780860477809TC5GENIChomozygous52666518
86047890060478901GA62GENIChomozygous52984655