chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51718395917183960AG45GENIChomozygous144358052
51718409917184100AG49GENIChomozygous144358053
51718509317185094TC58GENIChomozygous144358054
51718514417185145GT59GENIChomozygous144358055
51718551517185516GA45GENIChomozygous144358056
51718562317185624AG48GENIChomozygous147538387
51718595717185958TA49GENIChomozygous144358057
51718605517186056GA61GENIChomozygous144358058
51718612717186128GA62GENIChomozygous144358059
51718648817186489GA41GENIChomozygous147538388
51718650017186501TG41GENIChomozygous147538389
51718672217186723TC54GENIChomozygous144358060
51718694717186948AG57GENIChomozygous137389734
51718598817185989CG51GENIChomozygous137389732
51718532217185323TA46GENIChomozygous137389730
51718661817186619CG57GENIChomozygous137389733
51718695217186953AT59GENIChomozygous137389735
51718741917187420CT57GENIChomozygous144358061
51718761617187617CT60GENIChomozygous147538390
51718776317187764CT52GENIChomozygous147538391
51718792417187925TA39GENIChomozygous144358062
51718800917188010GA51GENIChomozygous147538392
51718598817185989CA51GENICheterozygous403133975