chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3124130185124130186GA19GENIChomozygous58390729
3124132088124132089A-13GENICpossibly homozygous58322345
3124132162124132163GA24GENIChomozygous58390730
3124132198124132199G-24GENIChomozygous58390731
3124132473124132474TC23GENIChomozygous57648765
3124133812124133813TC28GENIChomozygous57648769
3124133846124133847TC15GENIChomozygous57648771
3124134979124134980TC23GENIChomozygous57648773
3124135294124135295CCAG5GENICheterozygous58390732
3124135413124135414A-17GENIChomozygous58390733
3124136108124136109TC28GENIChomozygous58390734
3124136124124136125CG28GENIChomozygous58390735
3124136194124136195GA22GENIChomozygous57648777
3124136284124136285CT18GENIChomozygous57648779
3124136521124136522TC26GENIChomozygous58390736
3124136982124136983CT22GENIChomozygous57648783
3124137337124137338TC16GENIChomozygous57648787
3124137893124137894TC17GENIChomozygous57648789
3124138301124138307TTTTTT------8GENIChomozygous57648791
3124138709124138710CT17GENIChomozygous57648797
3124138965124138966AG27GENIChomozygous58390737
3124139265124139266TC20GENIChomozygous57648799
3124139288124139289GA23GENIChomozygous57648801
3124139445124139446AC19GENIChomozygous57648803
3124140240124140241GA20GENIChomozygous57648805
3124140398124140399CT22GENIChomozygous58390738
3124140579124140580AG27GENIChomozygous57648807
3124140997124140998AG23GENIChomozygous57648809
3124141069124141070CT18GENIChomozygous58390739
3124141073124141074AG19GENIChomozygous58390740
3124141200124141201AAGGGT15GENIChomozygous57648813
3124141214124141215AG18GENIChomozygous57648815
3124141219124141220GGC20GENIChomozygous57648817
3124141322124141323CT17GENIChomozygous57648819
3124141330124141335AAAAA-----10GENICheterozygous57648821
3124141348124141349TC10GENIChomozygous57648823
3124141542124141543TC16GENIChomozygous57648825
3124141645124141646CT20GENIChomozygous57648827
3124141329124141335AAAAAA------10GENICpossibly homozygous58032261