chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15650588156505882GA14GENIChomozygous146344006
15650610856506109CT13GENICpossibly homozygous135551774
15650836256508363AT35GENIChomozygous135551777
15650840356508404CT34GENIChomozygous135551778
15650914656509147CT51GENIChomozygous135551779
15651012356510124AG44GENIChomozygous135551780
15651174256511743GA34GENIChomozygous135551781
15651264456512645AT36GENIChomozygous135551782
15651466256514675TTTGATGTCTAAA42GENIChomozygous135406074
15650724656507248TT37GENIChomozygous135406072
15651264256512642T34GENIChomozygous135406073
15650977056509770GCGCT14GENICheterozygous143737436
15651536856515369G36GENICpossibly homozygous135406075
15651576556515766AT39GENIChomozygous135551783
15651630256516303GC36GENIChomozygous135551784
15651687656516877TC41GENIChomozygous135551785
15651700956517010AG38GENIChomozygous135551786
15651764256517643GA49GENIChomozygous135551787
15651809856518099CT36GENIChomozygous135551788
15652026556520266CT56GENIChomozygous135551789
15652027056520271AG55GENIChomozygous135551790
15652094556520946GA43GENIChomozygous135551791
15652101256521013CT38GENIChomozygous135551792
15652117456521175CT49GENIChomozygous135551793
15652293956522939A51GENIChomozygous135406076
15652358656523587CA40GENIChomozygous135551794
15652531556525316AG54GENIChomozygous135551795
15652488756524888A20GENICheterozygous144522120
15652387756523878GA34GENIChomozygous144541574