chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145549577145549578GA43GENIChomozygous113179030
4145549770145549774TGTC43GENIChomozygous130938738
4145549832145549832TT43GENIChomozygous130938739
4145549842145549842TGTGTGTGTGTGTGTCTGTGTATATATGCATCTGTATG46GENIChomozygous130938740
4145549851145549852TC39GENIChomozygous128136030
4145550319145550320AC51GENIChomozygous113179031
4145550569145550570GA48GENIChomozygous113179032
4145550868145550869GT56GENIChomozygous113179033
4145550931145550932AG50GENIChomozygous113179034
4145550995145550996AG52GENIChomozygous113179035
4145551013145551014GT50GENIChomozygous113179036
4145551188145551189TC54GENIChomozygous113179037
4145551276145551277GA45GENIChomozygous113179038
4145551513145551514AG52GENIChomozygous113179039
4145551516145551517AG52GENIChomozygous113179040
4145551729145551730TC55GENIChomozygous112871097
4145551739145551740AG57GENIChomozygous113179041
4145551806145551807GA58GENIChomozygous113179042
4145552266145552267TG40GENICpossibly homozygous113179043
4145552504145552505AT53GENIChomozygous112871098
4145552741145552742CA44GENIChomozygous113179044
4145552908145552909TC52GENIChomozygous113179045
4145553763145553763ATT50GENIChomozygous128088034
4145553948145553949GT38GENIChomozygous112871100
4145553961145553962GA40GENIChomozygous113179046
4145554224145554225AG48GENIChomozygous112871102
4145554280145554280AC44GENIChomozygous128088035
4145554622145554623AC40GENIChomozygous112871103
4145554856145554856T33GENIChomozygous130938741
4145554939145554940CT49GENIChomozygous112871105
4145554940145554941CG49GENIChomozygous112871106
4145554994145554994AC60GENIChomozygous128088037
4145555238145555239A65GENICpossibly homozygous128088038
4145555452145555453TC58GENIChomozygous112871107
4145555501145555502CT71GENICpossibly homozygous112871108
4145555710145555711AG71GENIChomozygous112871109
4145555932145555933CG69GENIChomozygous112871110