chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8111696985111696986CT18GENIChomozygous950347418
8111698864111698865GA5GENIChomozygous950347419
8111698989111698990GA17GENIChomozygous950347420
8111699188111699189CT16GENIChomozygous950347421
8111699841111699842GA26GENIChomozygous950347422
8111700229111700230AT8GENICpossibly homozygous950347423
8111700490111700491TC5GENIChomozygous950347424
8111700575111700576TC5GENIChomozygous950347425
8111701225111701226TC14GENIChomozygous950347426
8111701419111701420AG17GENIChomozygous950347427
8111701475111701476AG14GENIChomozygous950347428
8111702844111702845AT4GENIChomozygous950347429
8111703637111703638GC11GENIChomozygous950347430
8111703761111703762AT17GENIChomozygous950347431
8111704388111704389TG22GENIChomozygous950347432
8111704774111704775CT27GENIChomozygous950347433
8111706076111706077GC16GENIChomozygous950347434
8111706234111706235GA37GENIChomozygous950347435
8111708481111708482TC17GENIChomozygous950347436
8111709172111709173GC22GENIChomozygous950347437
8111710837111710838CT22GENIChomozygous950347438
8111713977111713978AG7GENIChomozygous950347439
8111714595111714596AG4GENIChomozygous950347440
8111716278111716279TG11GENIChomozygous950347441
8111717006111717007GA18GENIChomozygous950347442
8111719649111719650GT18GENIChomozygous950347443
8111720979111720980TC14GENIChomozygous950347444