chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142293282322932824GA30GENIChomozygous800250263
142293447722934478TC18GENIChomozygous800250264
142293448022934481AC19GENIChomozygous800250265
142293451722934518TC27GENIChomozygous800250266
142293764622937647TA38GENIChomozygous800250267
142294094922940950AG31GENIChomozygous800250268
142294134322941344CA15GENIChomozygous800250269
142294277722942778CA18GENIChomozygous800250270
142294389522943896AG25GENIChomozygous800250271
142294402922944030TA30GENIChomozygous800250272
142294751922947520CA17GENIChomozygous800250273
142294752122947522AC16GENIChomozygous800250274
142294884322948844GA25GENICpossibly homozygous800250275
142295235922952360CG25GENIChomozygous800250276
142295552222955523CT14GENIChomozygous800250277
142295557922955580GT19GENIChomozygous800250278