chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105934487559344876TC42GENIChomozygous116937596
105934937759349378TC23GENIChomozygous116607996
105935005459350055AG35GENIChomozygous116607998
105935354759353548CT22GENIChomozygous116608004
105935503759355038AG20GENIChomozygous116608006
105935596059355961AG40GENIChomozygous116608008
105935679459356795GA31GENICpossibly homozygous116788448
105935701259357013CT35GENIChomozygous116608010
105935701359357014AG35GENIChomozygous116608012
105935799059357991GA16GENIChomozygous116937598
105935863659358637CT16GENIChomozygous116608014
105935906559359066CT31GENIChomozygous116608016
105936004059360041TC28GENIChomozygous116608018
105936058459360585TA44GENIChomozygous116608020