chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51718395917183960AG34GENIChomozygous144358052
51718409917184100AG18GENIChomozygous144358053
51718509317185094TC19GENIChomozygous144358054
51718514417185145GT15GENIChomozygous144358055
51718532217185323TA17GENIChomozygous137389730
51718551517185516GA13GENIChomozygous144358056
51718595717185958TA17GENIChomozygous144358057
51718598817185989CG19GENIChomozygous137389732
51718605517186056GA17GENIChomozygous144358058
51718612717186128GA16GENIChomozygous144358059
51718661817186619CG12GENIChomozygous137389733
51718672217186723TC23GENIChomozygous144358060
51718694717186948AG21GENIChomozygous137389734
51718695217186953AT21GENIChomozygous137389735
51718741917187420CT22GENIChomozygous144358061
51718776317187764CT17GENIChomozygous147538391
51718562317185624AG18GENIChomozygous147538387
51718648817186489GA21GENIChomozygous147538388
51718650017186501TG19GENIChomozygous147538389
51718761617187617CT18GENIChomozygous147538390
51718792417187925TA13GENIChomozygous144358062
51718800917188010GA14GENIChomozygous147538392
51718598817185989CA19GENICheterozygous403133975