chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5106006453106006454GGC3GENIChomozygous55619974
5106006469106006470TTC1GENIChomozygous56442119
5106006621106006622CT1GENIChomozygous56549641
5106006624106006625TC1GENIChomozygous56549642
5106006987106006988CCG11GENIChomozygous55619979
5106007103106007104GA24GENIChomozygous55619980
5106007163106007164CT19GENICpossibly homozygous55619981
5106007397106007398GA31GENIChomozygous55619982
5106007960106007961T-23GENIChomozygous55619983
5106007964106007974TCCCTGAGGT----------24GENIChomozygous55619984
5106008075106008076CT17GENIChomozygous55619985
5106008122106008123TC10GENIChomozygous55619986