chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145549577145549578GA29GENIChomozygous113179030
4145550319145550320AC14GENIChomozygous113179031
4145550569145550570GA14GENIChomozygous113179032
4145550868145550869GT22GENICpossibly homozygous113179033
4145550931145550932AG26GENIChomozygous113179034
4145550995145550996AG21GENIChomozygous113179035
4145551013145551014GT22GENIChomozygous113179036
4145551188145551189TC21GENIChomozygous113179037
4145551276145551277GA30GENIChomozygous113179038
4145551513145551514AG6GENIChomozygous113179039
4145551516145551517AG6GENIChomozygous113179040
4145551729145551730TC15GENIChomozygous112871097
4145551739145551740AG17GENIChomozygous113179041
4145551806145551807GA20GENIChomozygous113179042
4145552266145552267TG19GENIChomozygous113179043
4145552504145552505AT28GENIChomozygous112871098
4145552741145552742CA23GENIChomozygous113179044
4145552908145552909TC22GENIChomozygous113179045
4145553948145553949GT20GENIChomozygous112871100
4145553961145553962GA24GENIChomozygous113179046
4145554224145554225AG19GENIChomozygous112871102
4145554622145554623AC22GENIChomozygous112871103
4145554939145554940CT25GENIChomozygous112871105
4145554940145554941CG25GENIChomozygous112871106
4145555452145555453TC9GENIChomozygous112871107
4145555501145555502CT11GENIChomozygous112871108
4145555710145555711AG13GENIChomozygous112871109
4145555932145555933CG6GENIChomozygous112871110