chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124157419841574198C25GENIChomozygous128990757
124157421541574216G26GENIChomozygous128990758
124157422141574222C25GENIChomozygous128990759
124157426441574264A16GENIChomozygous128990760
124157430441574304A14GENIChomozygous128990761
124157434141574341A13GENIChomozygous128990763
124157434541574345A13GENIChomozygous128990764
124157435541574355GC13GENIChomozygous128990765
124157436541574366CG12GENIChomozygous115385488
124157441741574417C14GENIChomozygous128990766
124157444041574440A15GENIChomozygous128990767
124157448841574489A15GENIChomozygous128990768
124157461341574614A17GENIChomozygous128990770
124157465141574652T17GENIChomozygous128990771
124157467041574670G17GENIChomozygous128990772
124157470641574706C17GENIChomozygous128990773
124157471841574719C17GENIChomozygous128990774
124157473241574733CT15GENIChomozygous115330721
124157473341574734TC15GENIChomozygous115704381
124157474241574742C15GENIChomozygous128990775
124157476841574770CC11GENIChomozygous128990777
124157479141574791C10GENIChomozygous128990779
124157479541574796C11GENIChomozygous128990780
124157480441574808GAAG11GENIChomozygous128990781
124157482541574826AC9GENIChomozygous115478047
124157482741574828GA9GENIChomozygous123638070
124157483241574833GT9GENIChomozygous115330723
124157484541574845C8GENIChomozygous128990782
124157485541574855AA9GENIChomozygous128990783
124157516941575169T12GENICheterozygous130582695