chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----13GENIChomozygous733002349
3154514276154514277TG14GENIChomozygous606271392
3154514414154514415AAGTCT15GENIChomozygous733002351
3154514475154514476TC15GENIChomozygous606271393
3154514477154514478TC16GENIChomozygous606271394
3154515475154515476GA13GENIChomozygous606271395
3154515681154515682TA15GENIChomozygous606271396
3154516008154516009GA15GENIChomozygous606271397
3154516009154516010AT15GENIChomozygous606271398
3154516260154516261TC28GENIChomozygous606271399
3154516884154516885AG32GENIChomozygous606271400
3154517077154517078TC25GENIChomozygous608209164
3154517156154517157AG28GENIChomozygous606271401
3154517593154517594TC21GENIChomozygous606271402
3154517632154517633G-22GENIChomozygous733002352
3154517898154517899TC26GENIChomozygous606271403
3154517982154517986GGCA----19GENIChomozygous733002353
3154518068154518069GA15GENIChomozygous606271404
3154518158154518159TTA25GENIChomozygous733002354
3154518562154518563CT29GENIChomozygous608209165
3154518737154518738AG22GENIChomozygous606271405
3154518931154518932GGT21GENICpossibly homozygous733002355
3154519100154519101CT24GENIChomozygous608209166
3154519184154519185CCA10GENICpossibly homozygous733002356
3154519315154519316CT15GENIChomozygous606271406
3154519896154519897CCTT21GENIChomozygous733002359
3154519985154519986AG15GENIChomozygous606271407
3154520058154520059TC21GENIChomozygous606271408
3154520781154520782TC21GENIChomozygous606271409
3154520987154520988CT22GENIChomozygous606271410
3154521914154521915TTAA15GENIChomozygous733002361
3154521930154521931AAC13GENICheterozygous733002362
3154522134154522135AG15GENIChomozygous606271411