chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71504526615045267AACTCTCTCT15GENICpossibly homozygous54956133
71504526715045269CT--15GENICheterozygous55216684
71504652815046529TG18GENIChomozygous53799405
71504700815047009AC16GENIChomozygous53799407
71504718815047189GA24GENIChomozygous53799409
71504749315047494CCCCT14GENIChomozygous53799410
71504808115048082AT18GENIChomozygous53799412
71505255015052551TC24GENIChomozygous53799422
71505255815052559TC24GENIChomozygous53799423
71505331915053320AC18GENIChomozygous53799425
71505628715056288GA24GENIChomozygous53799426
71505730315057304C-34GENIChomozygous53799428
71505760115057602GGAACA31GENIChomozygous53799429
71505800515058006TC28GENIChomozygous53799431
71505825115058252CCT7GENICpossibly homozygous53799433
71505842515058426GGTATAGA13GENIChomozygous53799438
71505882415058825G-23GENIChomozygous53799439
71505889515058896GA28GENIChomozygous53799441
71505966215059663GGA14GENIChomozygous53799443
71506054015060541GA32GENIChomozygous53799445
71506059515060596GA39GENIChomozygous53799447
71506066215060663AT23GENIChomozygous53799449
71506073015060731CT32GENIChomozygous53799450
71506073315060734TC31GENIChomozygous53799452
71506083215060833CT32GENIChomozygous53799454
71506084715060848AG26GENIChomozygous53799455
71506085615060857CG27GENIChomozygous53799457