chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123325722833257229TA9GENICheterozygous67295785
123325833033258331CA24GENIChomozygous66724774
123325887533258876TC25GENIChomozygous66724776
123325911033259111TC29GENIChomozygous66724778
123326188133261882AG8GENIChomozygous66724784
123326195833261959GC4GENIChomozygous66724786
123326203133262032GC8GENIChomozygous66724788
123326212733262128TC23GENIChomozygous66724790
123326224033262241TC32GENICpossibly homozygous66724792
123326224233262243TC33GENIChomozygous66724794
123326235033262351CG27GENIChomozygous66724796
123326247633262477TC26GENIChomozygous66724798
123326297733262978CT27GENIChomozygous66724801
123326301833263019AC28GENIChomozygous66724803
123326456033264561CG19GENIChomozygous66724811
123326481133264812GA11GENIChomozygous66724813
123326488933264890CT23GENICpossibly homozygous66724815
123326744233267443GA19GENIChomozygous66724817
123326782733267828TA7GENICheterozygous67295787
123326824733268248AG29GENIChomozygous66724819
123326890133268902GA23GENIChomozygous66724821
123327065433270655CG12GENIChomozygous66724823
123326191333261914CT5GENIChomozygous67183577