chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31063503510635036TC29GENIChomozygous111445105
31063576710635768TG16GENIChomozygous111445107
31063909510639107TCTCCACGCCGT16GENIChomozygous132038480
31064184410641845GA19GENIChomozygous111445127
31064213010642131CT17GENIChomozygous112065592
31064429510644296CT15GENIChomozygous112065594
31064624110646242CA22GENIChomozygous112065596
31065643810656439CG21GENIChomozygous111445193
31065703710657038GA25GENIChomozygous112065598
31066670810666710TT19GENIChomozygous127849106
31066853610668537CT12GENIChomozygous112065600
31067033310670334GA17GENIChomozygous112065602
31067085810670859CT18GENIChomozygous112065604
31067104910671053AAAC11GENIChomozygous127849107
31068002910680030TC15GENIChomozygous111445279
31068492510684926GA2GENICheterozygous112378717
31068561610685617C6GENIChomozygous130277326
31068562110685622C7GENIChomozygous132038481
31068585310685853C7GENIChomozygous127849115
31068611310686113TA7GENIChomozygous130277327
31068612410686124A9GENIChomozygous127849123
31068837810688379CT18GENIChomozygous111445295
31068947610689479CCC16GENIChomozygous127849124
31068984510689846AT22GENIChomozygous111445299
31069192310691924AG16GENIChomozygous111874887
31069209510692096TA19GENIChomozygous111445303
31069210910692110AG21GENIChomozygous111445305
31069356910693570CT17GENIChomozygous111445309
31069404210694049AAAAAAA33GENIChomozygous127849129
31069423410694235GA15GENIChomozygous111445311