chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143357284633572847GA40GENIChomozygous965030451
143357304933573050GA46GENIChomozygous965030452
143357331833573319TG32GENIChomozygous965030453
143357378933573790CT42GENIChomozygous965030454
143357381233573813AG41GENIChomozygous965030455
143357389733573898GA30GENIChomozygous965030456
143357409933574100AG24GENIChomozygous965030457
143357435933574360AG19GENIChomozygous965030458
143357451133574512TC39GENICpossibly homozygous965030459
143357464533574646AG45GENIChomozygous965030460
143357492433574925CT42GENIChomozygous965030461
143357563433575635CT35GENIChomozygous965030462
143357607033576071AG38GENIChomozygous965030463
143357611133576112TC31GENIChomozygous965030464
143357888533578886CG28GENIChomozygous965030465
143357911333579114AG24GENIChomozygous965030466
143357951133579512CT31GENIChomozygous965030467
143357954333579544CA34GENIChomozygous965030468
143358002833580029AG17GENIChomozygous965030469
143358020733580208TA16GENIChomozygous965030470
143358021433580215AG15GENIChomozygous965030471
143358055433580555AG6GENIChomozygous965030472
143358067133580672CG14GENIChomozygous965030473