chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045798744579875AG49GENIChomozygous109074755
2045802744580275GA45GENICpossibly homozygous109074757
2045814974581498CG16GENIChomozygous109074759
2045819864581987GA46GENICpossibly homozygous109074761
2045821194582120CT42GENIChomozygous109074763
2045826244582625CT44GENIChomozygous109233527
2045827214582722TA44GENIChomozygous109074765
2045828304582831GA44GENIChomozygous109074767
2045829564582957GT65GENICpossibly homozygous109074769
2045829954582996GA62GENIChomozygous109074771
2045832574583258CT53GENIChomozygous109074773
2045834684583469CA54GENIChomozygous109074775
2045835624583563GT50GENIChomozygous109074777
2045851984585199CT24GENIChomozygous109074779
2045815334581534CT8GENICheterozygous119757744
2045863384586339GA47GENIChomozygous109074781
2045865354586536TA44GENIChomozygous109074783
2045865434586544CA44GENIChomozygous109074785
2045866254586626CT48GENICpossibly homozygous109074787
2045867244586725AG24GENIChomozygous109074789
2045870634587064CT30GENIChomozygous109074791
2045890254589026GA52GENIChomozygous109074793
2045891694589170CT42GENICpossibly homozygous109074795
2045894224589423TC40GENIChomozygous109074797
2045906954590696CT38GENICpossibly homozygous109074799
2045908724590873GA43GENIChomozygous109074801
2045912304591231CT48GENIChomozygous109074803
2045913764591377AG24GENIChomozygous109074805
2045915054591506TC25GENIChomozygous109074807
2045920784592079GA46GENIChomozygous109074809
2045922724592273GA36GENICpossibly homozygous109074811
2045928004592801GA41GENIChomozygous109074813