chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37547880775478808TC32GENIChomozygous72000448
37547942375479424TG13GENIChomozygous72000450
37547971175479712AG18GENICpossibly homozygous72000452
37548081875480819CT14GENIChomozygous72000454
37548142475481425TC28GENIChomozygous72000458
37548190675481907AG22GENIChomozygous72000460
37548196575481966AG18GENIChomozygous72000462
37548219075482191GA20GENIChomozygous72000464
37548283475482835CT10GENIChomozygous72000466
37548346975483470TC27GENIChomozygous72000468
37548473175484732TG7GENIChomozygous72000470
37548682075486821CT25GENICpossibly homozygous72000472
37548702675487027AG21GENIChomozygous72000474
37548827975488280GA36GENIChomozygous72000480
37548915375489154GC26GENIChomozygous72000482
37548925475489255AG21GENICpossibly homozygous72000484
37548925975489260GA23GENICpossibly homozygous72000486
37548940375489404TC21GENIChomozygous72000488
37549004275490043GA16GENIChomozygous72000490
37549012875490129GA26GENIChomozygous72000492
37548775775487758TC22GENIChomozygous73041869
37549066575490666CT13GENIChomozygous72000494
37549149875491499CT32GENIChomozygous73041870
37549276175492762AG30GENIChomozygous72000496
37549280175492802AG31GENIChomozygous72000498
37549399575493996TC27GENIChomozygous72000502
37549591875495919AG26GENIChomozygous72000504