chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95277536852775369TA96GENICheterozygous508569362
95277541652775417CT66GENICheterozygous508569363
95277684152776842AG20GENIChomozygous507292040
95277764352777644AC62GENICpossibly homozygous507292041
95277829752778298TC49GENIChomozygous508569364
95277858952778590TC24GENIChomozygous508569365
95277884852778849AC14GENIChomozygous508569366
95277885952778860GA10GENIChomozygous508569367
95277892152778922A-10GENIChomozygous686035767
95277898852778989GC28GENIChomozygous508569368
95277928552779286GA52GENICpossibly homozygous508569369
95277934552779346GT57GENICheterozygous508569370
95277969052779691AG54GENICpossibly homozygous507292042
95277988452779885AG10GENIChomozygous507292043
95277995752779958AG21GENIChomozygous508569371
95278026552780266CT45GENICheterozygous508569372
95278026652780267CT44GENICheterozygous508569373
95278047652780477TC67GENICpossibly homozygous507292044
95278064552780646AG62GENIChomozygous507292045
95278092652780927AG52GENIChomozygous507292046
95278094052780941AG49GENIChomozygous507292047
95278107352781074TC60GENIChomozygous507292048
95278127252781273C-6GENIChomozygous686035768
95278188052781881TTA62GENIChomozygous686035769
95278294652782947GT73GENICpossibly homozygous507292049
95278338352783384TTG14GENICpossibly homozygous686035770
95278360252783603TC72GENIChomozygous507292050
95278385852783859CCGGGGG1GENIChomozygous686035772
95278388552783886TC35GENICpossibly homozygous507292051
95278409952784100AG91GENIChomozygous507292052