chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122782195327821954CA26GENIChomozygous50156179
122782235327822354CT23GENIChomozygous50156181
122782250427822505AG24GENIChomozygous50156183
122782256527822566AG17GENIChomozygous50156185
122782267727822678T-23GENIChomozygous50156187
122782300827823009TA16GENIChomozygous50156189
122782358527823586GA29GENIChomozygous50156191
122782391627823917CT13GENIChomozygous50156193
122782514627825147CT20GENIChomozygous50156197
122782473227824733GT25GENIChomozygous50156195
122782516627825186CAAGTCAACTCTTATAAAGG--------------------20GENIChomozygous50156199
122782544427825445TC16GENIChomozygous50156201
122782552927825530AG19GENIChomozygous50156203
122782628227826283GT22GENIChomozygous50156205
122782630027826301GA26GENIChomozygous50156207
122782642527826426GA15GENIChomozygous50156209
122782676027826761TC13GENIChomozygous50156211
122782701627827017TC17GENIChomozygous50156213
122782715827827159CA19GENIChomozygous50156215
122782717627827177CT23GENIChomozygous50156217
122782732527827326TA28GENIChomozygous50156219
122782754927827550GA17GENIChomozygous50156221
122782776927827770CT20GENIChomozygous50156223
122782797427827975CA22GENIChomozygous50156224
122782814827828149GA21GENIChomozygous50156226