chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71504526615045267AACTCTCTCT1GENIChomozygous54956133
71504652815046529TG25GENIChomozygous53799405
71504700815047009AC23GENIChomozygous53799407
71504718815047189GA30GENIChomozygous53799409
71504749315047494CCCCT12GENIChomozygous53799410
71504808115048082AT23GENIChomozygous53799412
71505255015052551TC26GENIChomozygous53799422
71505255815052559TC29GENIChomozygous53799423
71505331915053320AC20GENIChomozygous53799425
71505628715056288GA24GENIChomozygous53799426
71505730315057304C-22GENIChomozygous53799428
71505760115057602GGAACA23GENIChomozygous53799429
71505800515058006TC19GENIChomozygous53799431
71505825115058252CCT7GENIChomozygous53799433
71505842515058426GGTATAGA8GENIChomozygous53799438
71505882415058825G-8GENIChomozygous53799439
71505889515058896GA19GENIChomozygous53799441
71505966215059663GGA9GENICpossibly homozygous53799443
71506054015060541GA18GENIChomozygous53799445
71506059515060596GA23GENIChomozygous53799447
71506066215060663AT18GENIChomozygous53799449
71506073015060731CT19GENIChomozygous53799450
71506073315060734TC19GENIChomozygous53799452
71506083215060833CT22GENIChomozygous53799454
71506084715060848AG21GENIChomozygous53799455
71506085615060857CG21GENIChomozygous53799457