chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145549577145549578GA20GENIChomozygous113179030
4145550319145550320AC11GENIChomozygous113179031
4145550569145550570GA20GENIChomozygous113179032
4145550868145550869GT12GENIChomozygous113179033
4145550931145550932AG15GENIChomozygous113179034
4145550995145550996AG21GENIChomozygous113179035
4145551013145551014GT19GENIChomozygous113179036
4145551188145551189TC20GENIChomozygous113179037
4145551276145551277GA22GENIChomozygous113179038
4145551513145551514AG20GENIChomozygous113179039
4145551516145551517AG20GENIChomozygous113179040
4145551739145551740AG22GENIChomozygous113179041
4145551806145551807GA20GENIChomozygous113179042
4145552266145552267TG13GENIChomozygous113179043
4145552741145552742CA14GENIChomozygous113179044
4145552908145552909TC22GENIChomozygous113179045
4145553763145553763ATT15GENIChomozygous128088034
4145553948145553949GT16GENIChomozygous112871100
4145551729145551730TC21GENIChomozygous112871097
4145552504145552505AT14GENIChomozygous112871098
4145553961145553962GA18GENIChomozygous113179046
4145554224145554225AG17GENIChomozygous112871102
4145554280145554280AC23GENIChomozygous128088035
4145554622145554623AC17GENIChomozygous112871103
4145554856145554856T18GENIChomozygous130938741
4145554939145554940CT23GENIChomozygous112871105
4145554940145554941CG23GENIChomozygous112871106
4145554994145554994AC15GENIChomozygous128088037
4145555238145555239A25GENIChomozygous128088038
4145555452145555453TC26GENIChomozygous112871107
4145555501145555502CT23GENIChomozygous112871108
4145555710145555711AG25GENIChomozygous112871109
4145555932145555933CG25GENIChomozygous112871110