chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
94609597646095977GT27GENICpossibly homozygous117333876
94610973646109737GA26GENICpossibly homozygous117333877
94612004246120043TG7GENIChomozygous117333878
94612004446120045TG6GENIChomozygous117333879
94612004546120046TG5GENIChomozygous117333880
94613414246134143TG39GENICpossibly homozygous117333881