chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123325661733256618GA19GENICpossibly homozygous66724772
123325833033258331CA26GENIChomozygous66724774
123325887533258876TC45GENIChomozygous66724776
123325911033259111TC40GENIChomozygous66724778
123326116033261161AG9GENIChomozygous66724780
123326195833261959GC21GENIChomozygous66724786
123326212733262128TC31GENIChomozygous66724790
123326247633262477TC43GENIChomozygous66724798
123326297733262978CT18GENIChomozygous66724801
123326301833263019AC20GENIChomozygous66724803
123326456033264561CG24GENIChomozygous66724811
123326481133264812GA23GENIChomozygous66724813
123326488933264890CT21GENIChomozygous66724815
123326744233267443GA37GENIChomozygous66724817
123326824733268248AG27GENIChomozygous66724819
123326890133268902GA42GENIChomozygous66724821
123327065433270655CG36GENIChomozygous66724823