chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5146681778146681779TG10GENIChomozygous55773381
5146682146146682147GA9GENIChomozygous55773383
5146684724146684725TC8GENICpossibly homozygous55773385
5146685174146685175TC8GENIChomozygous55773387
5146692961146692962GA15GENIChomozygous55773389
5146693020146693021CT9GENIChomozygous55773391
5146693153146693154CT13GENIChomozygous55773393
5146695011146695012CCAT10GENICheterozygous55773395
5146695438146695439GA9GENIChomozygous55773402
5146695636146695637CT13GENIChomozygous55773404
5146696432146696433TC10GENIChomozygous55773406
5146696822146696823GA9GENIChomozygous55773408
5146698033146698035CC--10GENIChomozygous55773410
5146699959146699961TT--8GENIChomozygous55773412