chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----13GENIChomozygous709837246
3154514276154514277TG14GENIChomozygous565975695
3154514414154514415AAGTCT13GENIChomozygous709837248
3154514475154514476TC11GENIChomozygous565975696
3154514477154514478TC11GENIChomozygous565975697
3154515475154515476GA12GENIChomozygous565975698
3154515681154515682TA12GENIChomozygous565975699
3154516008154516009GA18GENIChomozygous565975700
3154516009154516010AT18GENIChomozygous565975701
3154516260154516261TC22GENIChomozygous565975702
3154516884154516885AG25GENIChomozygous565975703
3154517077154517078TC22GENIChomozygous568006920
3154517156154517157AG31GENIChomozygous565975704
3154517593154517594TC13GENIChomozygous565975705
3154517632154517633G-21GENIChomozygous709837249
3154517898154517899TC22GENIChomozygous565975706
3154517982154517986GGCA----16GENIChomozygous709837250
3154518068154518069GA16GENICpossibly homozygous565975707
3154518158154518159TTA28GENIChomozygous709837251
3154518562154518563CT19GENIChomozygous568006921
3154518737154518738AG17GENIChomozygous565975708
3154518931154518932GGT20GENICpossibly homozygous709837252
3154519100154519101CT10GENIChomozygous568006922
3154519184154519185CCA4GENIChomozygous709837253
3154519315154519316CT12GENIChomozygous565975709
3154519896154519897CCTT17GENIChomozygous709837256
3154519985154519986AG28GENIChomozygous565975710
3154520058154520059TC26GENIChomozygous565975711
3154520781154520782TC15GENIChomozygous565975712
3154520987154520988CT17GENIChomozygous565975713
3154521914154521915TTAA10GENIChomozygous709837258
3154521930154521931AAC12GENICheterozygous709837259
3154522134154522135AG16GENIChomozygous565975714