chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105639115856391159CA10GENIChomozygous116978056
105639906056399061AG55GENIChomozygous116783484
105639920956399210TC66GENIChomozygous116783486
105640150256401504GC14GENIChomozygous133680524
105640175556401756GT66GENIChomozygous116783490
105640200556402006T58GENIChomozygous131094486
105639497856394978TTCTG50GENICpossibly homozygous131094484
105640199256402000TTTTTTTG48GENICheterozygous131094485
105639816156398162CT59GENIChomozygous117059681
105639855156398552CT61GENIChomozygous117059683
105639970256399703CT71GENIChomozygous117059685
105640176156401762CA62GENIChomozygous117059687
105640274656402747TC60GENIChomozygous117059689