chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37547880775478808TC16GENIChomozygous72000448
37547942375479424TG28GENIChomozygous72000450
37547971175479712AG21GENIChomozygous72000452
37548081875480819CT27GENIChomozygous72000454
37548142475481425TC38GENIChomozygous72000458
37548190675481907AG19GENIChomozygous72000460
37548196575481966AG20GENIChomozygous72000462
37548219075482191GA20GENIChomozygous72000464
37548283475482835CT25GENIChomozygous72000466
37548346975483470TC31GENIChomozygous72000468
37548682075486821CT34GENICpossibly homozygous72000472
37548702675487027AG28GENIChomozygous72000474
37548827975488280GA41GENIChomozygous72000480
37548915375489154GC24GENIChomozygous72000482
37548925475489255AG16GENIChomozygous72000484
37548925975489260GA18GENIChomozygous72000486
37548940375489404TC18GENIChomozygous72000488
37548811575488116GA38GENIChomozygous74207068
37549004275490043GA27GENIChomozygous72000490
37549012875490129GA43GENIChomozygous72000492
37549066575490666CT31GENIChomozygous72000494
37549276175492762AG33GENIChomozygous72000496
37549311675493117GC25GENICpossibly homozygous74207074
37549399575493996TC23GENIChomozygous72000502
37549591875495919AG32GENIChomozygous72000504
37549629875496299AG24GENICpossibly homozygous74207077