chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116671647966716480TC16GENIChomozygous884165423
116671668466716685GA10GENIChomozygous884165424
116671730866717309TA8GENIChomozygous884165425
116671751166717512CG6GENIChomozygous884165426
116671755366717554CA20GENIChomozygous884165427
116671760366717604GC27GENIChomozygous884165428
116671771366717714GA16GENIChomozygous884165429
116671894366718944AG21GENIChomozygous884165430
116672232466722325CT20GENICheterozygous884165431
116672350966723510TC21GENIChomozygous884165432
116672411266724113AC27GENIChomozygous884165433
116672422866724229TC13GENIChomozygous884165434
116672543466725435TC23GENIChomozygous884165435
116672636166726362TC9GENICheterozygous884165436
116672675466726755GC17GENIChomozygous884165437
116672734666727347AG6GENIChomozygous884165438
116672886966728870CA3GENICheterozygous884165439
116672908866729089AT10GENIChomozygous884165440
116672969766729698TC22GENIChomozygous884165441
116673084166730842GA8GENIChomozygous884165442