chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14104340252104340253CT18GENIChomozygous113615429
14104341358104341359TC35GENIChomozygous113615430
14104352444104352445CT27GENIChomozygous113529823
14104346650104346651AG15GENIChomozygous113529805
14104347687104347688CA13GENIChomozygous113529807
14104348357104348358CT33GENIChomozygous113529809
14104349167104349168TC21GENIChomozygous113529811
14104349320104349321TC20GENIChomozygous113529813
14104349489104349490AG30GENIChomozygous113529815
14104349707104349708CG22GENIChomozygous113529817
14104350007104350008AT23GENIChomozygous113529819
14104351930104351931GT19GENIChomozygous113529821
14104353275104353276CT44GENIChomozygous113529827
14104354450104354451CT17GENIChomozygous113615431
14104357101104357102AT21GENIChomozygous113615432
14104357913104357914TC21GENIChomozygous113529829
14104358075104358076AG39GENIChomozygous113529831
14104360081104360082AG11GENIChomozygous113529833
14104360210104360211CA15GENIChomozygous113529835
14104360749104360750AT21GENIChomozygous113529837
14104360858104360859AG26GENIChomozygous113529839
14104363996104363997CA13GENIChomozygous113529841
14104364572104364573GA18GENIChomozygous113529843
14104365472104365473AG25GENIChomozygous113529845
14104366698104366699TC24GENIChomozygous113529847
14104370018104370019CA25GENIChomozygous113529849
14104370319104370320TC28GENIChomozygous113529851
14104371398104371399CT34GENIChomozygous113529857
14104371695104371696CG19GENIChomozygous113529859
14104371861104371862CG21GENIChomozygous113529861
14104371900104371901CT20GENIChomozygous113529863
14104375823104375824TC34GENIChomozygous113529865
14104354474104354475CA8GENIChomozygous113764669