chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123325418433254185CT11GENIChomozygous66724770
123325722833257229T10GENICheterozygous67337839
123325833033258331CA13GENIChomozygous66724774
123325838033258380T12GENIChomozygous67337840
123325887533258876TC8GENIChomozygous66724776
123325911033259111TC21GENIChomozygous66724778
123326116033261161AG8GENIChomozygous66724780
123326188133261882AG20GENIChomozygous66724784
123326197533261976A8GENIChomozygous67337841
123326203133262032GC13GENIChomozygous66724788
123326212733262128TC16GENIChomozygous66724790
123326215333262153C8GENIChomozygous67337842
123326217933262180G17GENIChomozygous67337843
123326224033262241TC6GENIChomozygous66724792
123326224233262243TC8GENIChomozygous66724794
123326235033262351CG19GENIChomozygous66724796
123326247633262477TC12GENIChomozygous66724798
123326297733262978CT17GENIChomozygous66724801
123326301833263019AC15GENIChomozygous66724803
123326456033264561CG16GENIChomozygous66724811
123326481133264812GA24GENIChomozygous66724813
123326744233267443GA6GENIChomozygous66724817
123326824733268248AG14GENIChomozygous66724819
123326890133268902GA29GENIChomozygous66724821
123327065433270655CG13GENIChomozygous66724823