chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121331059313310594GC21GENIChomozygous639131325
121331102613311027CG9GENIChomozygous639131326
121331105313311054CCT6GENICheterozygous750483668
121331299613312997TG30GENIChomozygous639131327
121331388313313884AG25GENIChomozygous639131328
121331393713313938GA15GENIChomozygous639131329
121331592413315925GA24GENICpossibly homozygous639131330
121331601913316020GC8GENICpossibly homozygous639131331
121331606813316069CCCCCATT13GENIChomozygous750483670
121331650113316503CC--19GENIChomozygous750483672
121331697913316980CT29GENIChomozygous639131332
121331846613318476TTGGAGAGGA----------28GENIChomozygous750483673
121331847813318481GAC---28GENIChomozygous750483674
121331877913318784GGTTC-----12GENICheterozygous750483675
121331893113318932GA28GENICpossibly homozygous639131333