chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123325661733256618GA11GENICheterozygous66724772
123325833033258331CA19GENIChomozygous66724774
123325887533258876TC16GENIChomozygous66724776
123325911033259111TC13GENIChomozygous66724778
123326195833261959GC10GENIChomozygous66724786
123326212733262128TC11GENIChomozygous66724790
123326247633262477TC11GENIChomozygous66724798
123326297733262978CT16GENIChomozygous66724801
123326301833263019AC18GENIChomozygous66724803
123326456033264561CG12GENIChomozygous66724811
123326481133264812GA8GENIChomozygous66724813
123326488933264890CT13GENIChomozygous66724815
123326744233267443GA16GENIChomozygous66724817
123326824733268248AG28GENIChomozygous66724819
123326890133268902GA19GENIChomozygous66724821
123327065433270655CG5GENIChomozygous66724823