chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2043825934382594TC9GENIChomozygous109233394
2043846934384694CA28GENIChomozygous109233395
2043855524385553CT23GENIChomozygous109233396
2043859544385955AG21GENIChomozygous109233397
2043877374387738TC22GENIChomozygous109233399
2043878444387845CT18GENIChomozygous109233400
2043888164388817CT11GENIChomozygous109233401
2043896484389649AG10GENIChomozygous109233402
2043898654389866GA8GENIChomozygous109233403
2043921024392103GA23GENIChomozygous109233405
2043923574392358CG18GENIChomozygous109233406
2043927924392793AC2GENIChomozygous109074380
2043927944392795AC2GENIChomozygous109074382
2043927964392797AC2GENIChomozygous109074384
2043927984392799AC2GENIChomozygous109074386
2043950904395091GC13GENIChomozygous109233407
2043951734395174GA10GENIChomozygous109296103
2043967104396711GA22GENIChomozygous109233408
2043968654396866GA15GENIChomozygous109233409
2043969874396988CA26GENIChomozygous109233410
2043971414397142CT19GENIChomozygous109233411
2043972974397298AG14GENIChomozygous109233412
2043978674397868AG9GENIChomozygous109233413
2043991474399148TC13GENIChomozygous109233415
2043996934399694TC17GENIChomozygous109233416
2043999704399971AG19GENIChomozygous109233417
2044001234400124GT19GENIChomozygous109233418
2044006254400626TC3GENIChomozygous109233419
2044010494401050TC10GENIChomozygous109074390
2044015084401509GA20GENIChomozygous109233421
2044015514401552GA23GENIChomozygous109233422