chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----2GENIChomozygous745410798
3154514276154514277TG13GENIChomozygous630672622
3154514414154514415AAGTCT4GENIChomozygous745410800
3154514475154514476TC5GENIChomozygous630672623
3154514477154514478TC5GENIChomozygous630672624
3154515475154515476GA18GENICpossibly homozygous630672625
3154515681154515682TA16GENICheterozygous630672626
3154516008154516009GA6GENICheterozygous630672627
3154516009154516010AT5GENICheterozygous630672628
3154516260154516261TC9GENIChomozygous630672629
3154516884154516885AG15GENICpossibly homozygous630672630
3154517077154517078TC16GENICpossibly homozygous630672631
3154517156154517157AG19GENICpossibly homozygous630672632
3154517593154517594TC15GENICheterozygous630672633
3154517632154517633G-6GENIChomozygous745410801
3154517898154517899TC18GENIChomozygous630672634
3154517982154517986GGCA----10GENICheterozygous745410802
3154518068154518069GA12GENIChomozygous630672635
3154518158154518159TTA19GENIChomozygous745410803
3154518562154518563CT30GENIChomozygous630672636
3154518737154518738AG17GENICpossibly homozygous630672637
3154519100154519101CT17GENIChomozygous630672638
3154519184154519185CCA5GENIChomozygous745410804
3154519315154519316CT20GENICpossibly homozygous630672639
3154519985154519986AG9GENICpossibly homozygous630672640
3154520058154520059TC20GENIChomozygous630672641
3154520781154520782TC18GENIChomozygous630672642
3154520987154520988CT17GENICpossibly homozygous630672643
3154521914154521915TTAA2GENICheterozygous745410807
3154522134154522135AG23GENICpossibly homozygous630672644