chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15650724656507248TT49GENIChomozygous135406072
15650836256508363AT51GENIChomozygous135551777
15650840356508404CT57GENIChomozygous135551778
15650914656509147CT61GENIChomozygous135551779
15651012356510124AG60GENIChomozygous135551780
15651174256511743GA52GENIChomozygous135551781
15651264256512642T42GENIChomozygous135406073
15651264456512645AT43GENIChomozygous135551782
15651466256514675TTTGATGTCTAAA46GENIChomozygous135406074
15651536856515369G48GENIChomozygous135406075
15651576556515766AT48GENIChomozygous135551783
15651630256516303GC43GENIChomozygous135551784
15651687656516877TC33GENIChomozygous135551785
15651700956517010AG38GENIChomozygous135551786
15651764256517643GA44GENIChomozygous135551787
15651809856518099CT52GENIChomozygous135551788
15652026556520266CT47GENIChomozygous135551789
15652027056520271AG45GENIChomozygous135551790
15652094556520946GA59GENIChomozygous135551791
15652101256521013CT69GENIChomozygous135551792
15652117456521175CT59GENIChomozygous135551793
15652293956522939A43GENIChomozygous135406076
15652358656523587CA57GENIChomozygous135551794
15652531556525316AG57GENIChomozygous135551795
15652387756523878GA31GENIChomozygous144541574
15652488756524888A11GENICheterozygous144522120