chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113525138535251386GA19GENIChomozygous50729040
113525359735253598GA21GENICpossibly homozygous50729041
113525417835254179TG18GENIChomozygous50729044
113525439335254394TC34GENICpossibly homozygous50729045
113525480635254807CT12GENIChomozygous50729046
113525503735255038TTACACACACACACAC1GENIChomozygous51179632
113525510435255105TC32GENIChomozygous50729049
113525567935255682TTG---14GENIChomozygous50729050
113525971535259716TA20GENICpossibly homozygous50729053
113525987435259875AAC1GENIChomozygous50729054
113525997735259978GGTT3GENICheterozygous50729055
113526064435260645GA28GENICpossibly homozygous50729056
113526162935261630TA23GENIChomozygous50729059
113526185635261857GA29GENIChomozygous50729060
113526273935262740AT21GENIChomozygous50729061
113526334635263347GA20GENICpossibly homozygous50729062
113526353335263534AT21GENICpossibly homozygous50729063
113526368935263690GA28GENICpossibly homozygous50729064
113526378335263784TG18GENIChomozygous50729065
113526541135265412GA4GENICheterozygous50729067
113526632035266321G-15GENIChomozygous50729076
113526661135266612AG18GENIChomozygous50729077
113526816935268170TC27GENIChomozygous50729078