chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131848172131848173CT12GENICpossibly homozygous56232452
5131848895131848896TA4GENICheterozygous56232453
5131849138131849139AT2GENIChomozygous56232454
5131852832131852833CA13GENICheterozygous56232457
5131853075131853076GGT9GENIChomozygous55726575
5131853165131853166AG15GENIChomozygous55726577
5131853887131853888GT3GENICheterozygous55726583