chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131848172131848173CT23GENICpossibly homozygous56232452
5131848895131848896TA10GENIChomozygous56232453
5131848946131848947AAAGAGAGAGAGAGAG4GENIChomozygous56452342
5131849138131849139AT7GENIChomozygous56232454
5131850735131850736CCGTGTGTGT15GENIChomozygous56531742
5131852534131852535TTCTCC4GENIChomozygous56531744
5131852832131852833CA30GENIChomozygous56232457
5131853075131853076GGT29GENIChomozygous55726575
5131853165131853166AG18GENIChomozygous55726577
5131853887131853888GT18GENIChomozygous55726583
5131853990131853991CCTTTTTTT7GENIChomozygous56531746