chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
731182743118275GC22GENICpossibly homozygous53768143
731185993118600CT21GENIChomozygous53768145
731188003118801TC26GENICpossibly homozygous53768147
731192773119278GA16GENICheterozygous53768153
731207033120704A-2GENICheterozygous53768157
731214273121428GC2GENIChomozygous53768159
731215443121545GA8GENIChomozygous53768161
731216903121691AG16GENIChomozygous53768163
731217403121741TC20GENICheterozygous53768165
731225293122530GGA12GENICpossibly homozygous53768167
731238623123863GGT4GENICheterozygous53768169
731253413125342GA9GENICpossibly homozygous53768178
731259213125922TC5GENICheterozygous53768185
731281513128152AACACAGGGAGATCCCTGGGCT3GENICheterozygous53768189
731286563128657CG24GENICheterozygous53768193
731293013129303GG--1GENIChomozygous53768195
731314293131430CT23GENICheterozygous53768199
731332293133230TTC2GENIChomozygous53768202
731347423134743GA22GENICpossibly homozygous53768204
731387423138743GA6GENICheterozygous53768216
731398753139876GA28GENICpossibly homozygous53768218
731401113140112TC14GENICpossibly homozygous53768220
731414023141403AACGGAGGGTGT1GENIChomozygous53768222