chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113525138535251386GA13GENIChomozygous50729040
113525359735253598GA21GENIChomozygous50729041
113525417835254179TG15GENIChomozygous50729044
113525439335254394TC22GENICpossibly homozygous50729045
113525480635254807CT16GENICpossibly homozygous50729046
113525510435255105TC24GENIChomozygous50729049
113525567935255682TTG---7GENIChomozygous50729050
113525971535259716TA16GENICpossibly homozygous50729053
113525997735259978GGTT1GENIChomozygous50729055
113526064435260645GA18GENICpossibly homozygous50729056
113526162935261630TA14GENIChomozygous50729059
113526185635261857GA19GENICpossibly homozygous50729060
113526265235262653A-4GENICheterozygous51240303
113526273935262740AT14GENICpossibly homozygous50729061
113526334635263347GA23GENICpossibly homozygous50729062
113526353335263534AT17GENICpossibly homozygous50729063
113526368935263690GA20GENICpossibly homozygous50729064
113526378335263784TG13GENICpossibly homozygous50729065
113526541135265412GA7GENICheterozygous50729067
113526632035266321G-12GENIChomozygous50729076
113526661135266612AG20GENICpossibly homozygous50729077
113526816935268170TC18GENIChomozygous50729078