chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
498818419881842AC41GENIChomozygous112492720
498821159882116GT35GENIChomozygous112492722
498823949882395GA66GENIChomozygous112492724
498826919882692AG46GENIChomozygous112492726
498827329882733AC42GENIChomozygous112492728
498828159882816CT34GENICpossibly homozygous112492730
498829369882937TC37GENIChomozygous112492731
498831699883170AC27GENIChomozygous112492733
498839749883975TC54GENIChomozygous112492735
498840489884049TA58GENIChomozygous112492737
498855309885531GA37GENIChomozygous112492739
498856899885690GA44GENIChomozygous112492741
498857889885789GA57GENIChomozygous112492743
498873249887325GA13GENICpossibly homozygous112492745
498873329887333GA11GENICheterozygous112492747
498873529887353AG8GENICpossibly homozygous112492749
498890459889046GA44GENIChomozygous112492753
498899719889972CT44GENIChomozygous112492755
498907689890769AG38GENIChomozygous112492757
498908559890856CT40GENIChomozygous112492759
498915369891537TG22GENIChomozygous112492761
498928609892861AG52GENIChomozygous112492763
498940089894009CT37GENIChomozygous112492765
498970109897011CT42GENIChomozygous112492767
498977069897707TC30GENIChomozygous112492769
498982009898201TC26GENIChomozygous112492771
498996379899638TA47GENIChomozygous112492773
498997189899719AG48GENIChomozygous112492775
499013869901387GA7GENIChomozygous112492777
499017529901753AG36GENICpossibly homozygous112492779
499022829902283TC38GENIChomozygous112492781
499027559902756CT24GENIChomozygous112492785
499028959902896AG40GENIChomozygous112492787
499046039904604AG47GENIChomozygous112492789
499048079904808TC37GENIChomozygous112492791
499050639905064CT33GENIChomozygous112492793
499060069906007GA33GENIChomozygous112492795
499062269906227AG39GENIChomozygous112492797
499079809907981CT30GENIChomozygous112492799
499031669903167TC39GENICheterozygous113250910
499013679901368GA3GENICheterozygous113250908
499031199903120CT50GENICheterozygous113250909