chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167084030570840305T42GENIChomozygous129378181
167084148770841488A54GENIChomozygous129378182
167084152970841529G53GENIChomozygous129378183
167084156470841565T53GENIChomozygous129378184
167084159070841591A55GENIChomozygous129378185
167084164570841646AT57GENIChomozygous119127559
167084167370841674G54GENIChomozygous129378186
167084173270841733T47GENIChomozygous129378187
167084173970841739C47GENIChomozygous129378188
167084178370841784A52GENIChomozygous129378189
167084193870841938C38GENIChomozygous129378190
167084198070841980G38GENIChomozygous129378191
167084198470841985C38GENIChomozygous129378192
167084199070841991C40GENIChomozygous129378193
167084223070842230C49GENIChomozygous129378194
167084227170842272G53GENIChomozygous129378195
167084227870842279C50GENIChomozygous129378196
167084230370842304T45GENIChomozygous129378197
167084231970842320AT44GENIChomozygous119127560
167084234170842342T41GENIChomozygous129378198
167084234870842348A41GENIChomozygous129378199
167084235470842354A39GENIChomozygous129378200
167084237070842371A30GENIChomozygous129378201
167084237370842374C30GENIChomozygous129378202
167084237870842379C29GENIChomozygous129378203
167084240370842403G21GENIChomozygous129378204
167084241170842411C18GENIChomozygous129378205
167084242270842423TC12GENIChomozygous124249557
167084242470842425CT10GENIChomozygous124249558
167084243170842431T8GENIChomozygous129378206
167084244270842443TA5GENIChomozygous124249560
167084244570842446CT5GENIChomozygous124249561
167084245170842452C4GENIChomozygous129378207
167084337970843379C2GENIChomozygous129378210
167084339170843391T2GENIChomozygous129378211
167084186270841863GA57GENIChomozygous112176981
167084239170842392GT25GENIChomozygous112176983
167084214770842148TA55GENICpossibly homozygous112025151
167084346070843461C2GENIChomozygous130159754
167084689670846897T38GENICheterozygous130159755