chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101110111611101117CG11GENIChomozygous116993928
101110123311101234GA18GENIChomozygous116993929
101110294911102950AG29GENIChomozygous116494204
101110319011103191TG30GENIChomozygous116494206
101110444811104449CT23GENIChomozygous116993930
101110504011105041TC23GENIChomozygous116494210
101110605811106059CA10GENIChomozygous116494212
101110922311109224GA22GENIChomozygous116494222
101111013111110132GA19GENIChomozygous116494224
101111234511112346CT16GENIChomozygous116993931
101111247711112478TC22GENIChomozygous116494230
101111342811113429CT10GENIChomozygous116993932
101111409211114093CT13GENIChomozygous116494234
101111438611114387TC21GENIChomozygous116494238
101111610811116109GT14GENIChomozygous116494240
101111611011116111TC15GENIChomozygous116494242
101111742211117423TC6GENIChomozygous116494244
101111750511117506TC15GENIChomozygous116494246
101111775411117755GT9GENIChomozygous116494248
101111814511118146CT17GENIChomozygous116494252
101111935411119355CT19GENIChomozygous116993933
101112223911122240CT4GENIChomozygous116494260
101112306411123065AG3GENIChomozygous116494262
101112440511124406GA15GENIChomozygous116993934
101112535811125359TC16GENIChomozygous116494268
101112551811125519GA14GENIChomozygous116494270
101113008511130086TC5GENIChomozygous116494272
101113188611131887GA11GENIChomozygous116993935
101113193911131940AG12GENIChomozygous116494276
101113326011133261GA13GENIChomozygous116993936
101113406211134063GA17GENIChomozygous116993937
101113656911136570CT15GENIChomozygous116494282
101113711611137117GT10GENIChomozygous116734230
101113721611137217GC9GENIChomozygous116494284
101113917911139180GA15GENIChomozygous116993939
101114079311140794CT22GENIChomozygous116993940
101114142411141425TC22GENIChomozygous116734236
101114183611141837GC21GENIChomozygous116734238
101114263811142639GA15GENIChomozygous116734240
101114273711142738GA15GENICpossibly homozygous116993941
101114342611143427GA16GENIChomozygous116993942
101114361411143615TC12GENIChomozygous116858837