chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135121921851219219AC28GENIChomozygous114342877
135121936151219362GA16GENIChomozygous114672302
135121982251219823TA39GENIChomozygous114342879
135122087351220874AG27GENIChomozygous114342881
135122092051220921CT21GENIChomozygous114342883
135122135551221356TC28GENIChomozygous114342885
135122189251221893TC31GENIChomozygous114342887
135122235651222357CT26GENICpossibly homozygous114342889
135122283051222831TC32GENIChomozygous114342891
135122294651222947TC38GENIChomozygous114342893
135122304751223048TA31GENIChomozygous114342895
135122373951223740CA30GENIChomozygous114342897
135122430751224308CT34GENIChomozygous114342899