chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98267692082676921AG25GENIChomozygous120280108
98268002382680024GA28GENIChomozygous117588909
98268200182682002AT16GENIChomozygous117588913
98268324182683242GT34GENIChomozygous117588915
98268531482685315CT35GENIChomozygous120280109
98268735582687356CT16GENIChomozygous120280110
98269116282691163CT35GENICpossibly homozygous120280111
98269215682692157CT37GENIChomozygous120280112
98269276882692769TC41GENIChomozygous117588925
98269299582692996TC22GENIChomozygous117588927
98269348082693481TC23GENIChomozygous117588929
98269425182694252CT24GENIChomozygous120280113
98269685682696857AC33GENIChomozygous117588935
98269749082697491AG24GENIChomozygous117588937
98269780382697804TC20GENIChomozygous117588939
98269832782698328CG19GENIChomozygous117588941
98269883582698836CA15GENIChomozygous120280114