chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166999479166999480TC21GENIChomozygous108357376
1166999495166999496CT21GENIChomozygous108357377
1166999799166999800GA17GENIChomozygous109522786
1167000311167000312AG21GENIChomozygous108357378
1167004653167004654TG21GENIChomozygous109522787
1167005073167005074TC16GENIChomozygous109522788
1167007384167007385TC30GENIChomozygous108955378
1167007763167007764AC29GENIChomozygous108357389
1167007845167007846TC24GENIChomozygous108955379
1167009316167009317CT11GENIChomozygous108357390
1167009532167009533TC20GENIChomozygous108357391
1167009857167009858TC18GENIChomozygous108357392
1167010011167010012GA15GENIChomozygous108357393
1167010017167010018AG14GENIChomozygous108357394
1167011313167011314AG25GENIChomozygous108357396
1167011419167011420AG19GENIChomozygous108357397
1167011457167011458AG21GENIChomozygous108357398
1167011853167011854CT20GENIChomozygous108955386
1167011955167011956TG20GENIChomozygous108357399
1167013919167013920CT20GENIChomozygous109522789