chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121326150813261509AG21GENICpossibly homozygous50363316
121326190513261906T-1GENIChomozygous50059189
121326205613262057CG1GENIChomozygous50363318
121326219513262196GC14GENICpossibly homozygous50363320
121326266913262670TC8GENIChomozygous50059199
121326283613262837CCAA1GENIChomozygous50059201
121326356613263567CT21GENIChomozygous50363322
121326360613263607CT11GENICpossibly homozygous50363324
121326367013263671AG4GENIChomozygous50281086
121326368113263682TTGG1GENIChomozygous50363326
121326392613263935TTTTTCTTT---------2GENICheterozygous50503829
121326477013264771TC26GENICpossibly homozygous50059217
121326490013264901CT11GENIChomozygous50281087
121326491213264913AG9GENIChomozygous50059219
121326492713264928AG7GENIChomozygous50059221
121326590013265901GA16GENICpossibly homozygous50059229
121326618213266183TC8GENIChomozygous50059237
121326710213267103GA23GENIChomozygous50059239
121326726713267268TC13GENIChomozygous50059241
121326728413267285TC14GENIChomozygous50059243