chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----8GENIChomozygous687231403
3154514276154514277TG10GENIChomozygous511433578
3154514414154514415AAGTCT13GENIChomozygous687231404
3154514475154514476TC14GENIChomozygous511433579
3154514477154514478TC15GENIChomozygous511433580
3154515475154515476GA14GENIChomozygous511433581
3154515681154515682TA15GENIChomozygous511433582
3154516260154516261TC27GENIChomozygous511433583
3154516884154516885AG33GENIChomozygous511433584
3154517077154517078TC24GENIChomozygous513804182
3154517156154517157AG26GENIChomozygous511433585
3154517593154517594TC21GENIChomozygous511433586
3154517632154517633G-21GENIChomozygous687231405
3154517898154517899TC26GENIChomozygous511433587
3154517982154517986GGCA----19GENIChomozygous687231406
3154518068154518069GA12GENIChomozygous511433588
3154518158154518159TTA25GENIChomozygous687231407
3154518562154518563CT29GENIChomozygous513804183
3154518737154518738AG23GENIChomozygous511433589
3154518931154518932GGT20GENIChomozygous687231408
3154519100154519101CT27GENIChomozygous513804184
3154519184154519185CCA13GENICpossibly homozygous687231409
3154519184154519185CCCA13GENICheterozygous687231410
3154519315154519316CT20GENIChomozygous511433590
3154519630154519636TCCCTC------19GENICheterozygous687231411
3154519645154519646CG24GENICpossibly homozygous511433591
3154519651154519652GC23GENIChomozygous511433592
3154519896154519897CCTT9GENIChomozygous687231413
3154519985154519986AG16GENIChomozygous511433593
3154520058154520059TC24GENIChomozygous511433594
3154520781154520782TC22GENIChomozygous511433595
3154520987154520988CT22GENIChomozygous511433596
3154521914154521915TTAA15GENIChomozygous687231414
3154521930154521931AAC18GENICheterozygous687231415
3154521931154521932AC18GENICheterozygous511433597
3154522134154522135AG16GENIChomozygous511433598