chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123325417433254175CT43GENICheterozygous66724768
123325418433254185CT42GENICheterozygous66724770
123325503933255040CT46GENICheterozygous67491343
123325508133255082TC51GENICheterozygous67698219
123325661733256618GA32GENICheterozygous66724772
123325833033258331CA42GENIChomozygous66724774
123325887533258876TC39GENIChomozygous66724776
123325911033259111TC30GENIChomozygous66724778
123326116033261161AG9GENIChomozygous66724780
123326185833261859GC5GENIChomozygous66724782
123326188133261882AG11GENIChomozygous66724784
123326195833261959GC19GENIChomozygous66724786
123326203133262032GC12GENIChomozygous66724788
123326212733262128TC5GENIChomozygous66724790
123326224033262241TC27GENIChomozygous66724792
123326224233262243TC29GENIChomozygous66724794
123326235033262351CG35GENIChomozygous66724796
123326247633262477TC38GENIChomozygous66724798
123326297733262978CT30GENIChomozygous66724801
123326301833263019AC28GENIChomozygous66724803
123326413933264140GA28GENICheterozygous66724805
123326414433264145GA31GENICheterozygous66724807
123326456033264561CG29GENIChomozygous66724811
123326481133264812GA31GENIChomozygous66724813
123326488933264890CT34GENICpossibly homozygous66724815
123326744233267443GA34GENIChomozygous66724817
123326824733268248AG30GENIChomozygous66724819
123326890133268902GA53GENIChomozygous66724821
123327065433270655CG25GENIChomozygous66724823