chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045798744579875AG54GENIChomozygous109074755
2045802744580275GA63GENICpossibly homozygous109074757
2045814974581498CG28GENIChomozygous109074759
2045819864581987GA51GENICpossibly homozygous109074761
2045821194582120CT59GENICpossibly homozygous109074763
2045826244582625CT45GENIChomozygous109233527
2045827214582722TA51GENICpossibly homozygous109074765
2045828304582831GA65GENIChomozygous109074767
2045829564582957GT57GENIChomozygous109074769
2045829954582996GA56GENIChomozygous109074771
2045832574583258CT42GENIChomozygous109074773
2045834684583469CA47GENICpossibly homozygous109074775
2045835624583563GT48GENIChomozygous109074777
2045851984585199CT40GENICpossibly homozygous109074779
2045863384586339GA43GENIChomozygous109074781
2045865354586536TA41GENIChomozygous109074783
2045865434586544CA40GENIChomozygous109074785
2045866254586626CT37GENIChomozygous109074787
2045867244586725AG47GENIChomozygous109074789
2045870634587064CT58GENIChomozygous109074791
2045890254589026GA54GENIChomozygous109074793
2045891694589170CT63GENICpossibly homozygous109074795
2045894224589423TC43GENICpossibly homozygous109074797
2045906954590696CT63GENIChomozygous109074799
2045908724590873GA60GENIChomozygous109074801
2045912304591231CT77GENIChomozygous109074803
2045913764591377AG60GENIChomozygous109074805
2045915054591506TC46GENIChomozygous109074807
2045920784592079GA61GENIChomozygous109074809
2045922724592273GA44GENICpossibly homozygous109074811
2045928004592801GA37GENIChomozygous109074813