chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2142481904142481910ACACAC------2GENIChomozygous704465671
2142482409142482410G-8GENICpossibly homozygous704465672
2142482816142482817AC27GENIChomozygous557247598
2142482888142482889CT21GENIChomozygous557247599
2142483162142483163TC32GENIChomozygous557247600
2142485687142485688GGTGGAGGAGCATGC35GENIChomozygous704465673
2142485963142485964A-22GENIChomozygous704465674
2142487041142487042TTTTGA35GENIChomozygous704465675
2142487131142487132CA32GENIChomozygous557247601
2142487539142487540CCAACTCTCAGTTCCTTTCTCCCG26GENIChomozygous704465676
2142487741142487742AT29GENIChomozygous557247602
2142488627142488628GT24GENIChomozygous557247603
2142488738142488739AG21GENIChomozygous557247604
2142488780142488781GA23GENIChomozygous557247605
2142489078142489079GGAAA10GENIChomozygous704465679
2142489749142489750TC33GENIChomozygous557247606
2142490080142490081C-30GENIChomozygous704465680
2142490293142490294CT19GENIChomozygous557247607
2142491308142491309CT30GENICpossibly homozygous557247608
2142492423142492424T-10GENIChomozygous704465681
2142492568142492569TTTTTTC8GENIChomozygous704465682
2142495236142495237GA31GENIChomozygous557247609
2142495992142495993A-6GENIChomozygous704465683
2142496006142496007A-9GENIChomozygous704465684
2142496158142496159TTGG10GENIChomozygous704465685
2142497646142497647AT28GENIChomozygous557247610
2142497727142497728CT24GENIChomozygous557247611