chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2174013005174013006A31GENIChomozygous135961046
2174013019174013020GA33GENIChomozygous142964734
2174015461174015462CA74GENIChomozygous142964735
2174017789174017790CT66GENIChomozygous142964736
2174017885174017886CG64GENIChomozygous142964737
2174018006174018007CT66GENIChomozygous142964738
2174018837174018838GA47GENIChomozygous142964739
2174019042174019043TC55GENIChomozygous142964740
2174017474174017475C50GENICpossibly homozygous142900925
2174019230174019231G54GENIChomozygous142900926
2174017994174017995TA62GENIChomozygous136372649
2174018174174018175TC45GENIChomozygous136372650
2174021083174021084AG61GENIChomozygous136372652
2174021555174021556CT46GENIChomozygous142964741
2174022078174022079AG47GENIChomozygous142964742
2174025769174025770GA59GENIChomozygous142964743
2174026086174026087AG62GENIChomozygous136372653
2174027571174027572TA59GENIChomozygous136372655
2174023861174023862C31GENICheterozygous403027871
2174023856174023858AT31GENIChomozygous142900927
2174026305174026305GGAA52GENICpossibly homozygous142900928
2174027021174027024CTC67GENIChomozygous142900929
2174023920174023921CA20GENICheterozygous154014937
2174023920174023921C20GENIChomozygous404057999
2174023861174023862CT31GENIChomozygous403027872