chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123325417433254175CT26GENICheterozygous66724768
123325661733256618GA17GENICheterozygous66724772
123325833033258331CA25GENIChomozygous66724774
123325887533258876TC25GENIChomozygous66724776
123325911033259111TC19GENIChomozygous66724778
123326116033261161AG14GENIChomozygous66724780
123326185833261859GC2GENIChomozygous66724782
123326188133261882AG2GENIChomozygous66724784
123326195833261959GC1GENIChomozygous66724786
123326203133262032GC3GENIChomozygous66724788
123326212733262128TC5GENIChomozygous66724790
123326224033262241TC10GENIChomozygous66724792
123326224233262243TC10GENIChomozygous66724794
123326235033262351CG21GENIChomozygous66724796
123326236033262361CA23GENIChomozygous66853163
123326247633262477TC23GENIChomozygous66724798
123326297733262978CT16GENIChomozygous66724801
123326301833263019AC16GENIChomozygous66724803
123326413933264140GA26GENICheterozygous66724805
123326414433264145GA27GENICheterozygous66724807
123326414833264149GA29GENICheterozygous66724809
123326456033264561CG16GENIChomozygous66724811
123326481133264812GA26GENIChomozygous66724813
123326488933264890CT33GENICpossibly homozygous66724815
123326744233267443GA25GENIChomozygous66724817
123326824733268248AG24GENIChomozygous66724819
123326890133268902GA31GENIChomozygous66724821
123327065433270655CG23GENICpossibly homozygous66724823