chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51718395917183960AG53GENIChomozygous144358052
51718409917184100AG50GENIChomozygous144358053
51718509317185094TC42GENIChomozygous144358054
51718514417185145GT39GENIChomozygous144358055
51718532217185323TA45GENIChomozygous137389730
51718551517185516GA44GENIChomozygous144358056
51718595717185958TA41GENIChomozygous144358057
51718598817185989CG41GENIChomozygous137389732
51718598817185989CA41GENICheterozygous403133975
51718605517186056GA44GENIChomozygous144358058
51718612717186128GA40GENICpossibly homozygous144358059
51718661817186619CG38GENIChomozygous137389733
51718672217186723TC37GENIChomozygous144358060
51718694717186948AG46GENIChomozygous137389734
51718695217186953AT45GENIChomozygous137389735
51718761617187617CT54GENIChomozygous147538390
51718562317185624AG54GENICpossibly homozygous147538387
51718648817186489GA47GENIChomozygous147538388
51718650017186501TG45GENIChomozygous147538389
51718741917187420CT43GENIChomozygous144358061
51718776317187764CT39GENIChomozygous147538391
51718792417187925TA52GENIChomozygous144358062
51718800917188010GA48GENIChomozygous147538392