chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2050713885071389CA10GENIChomozygous125176934
2050714925071493AT27GENIChomozygous125176935
2050716575071658GA22GENIChomozygous125176936
2050719445071945AG34GENIChomozygous125176937
2050721825072183CA30GENIChomozygous125176938
2050722085072209CT25GENIChomozygous125176939
2050722535072254TC12GENICheterozygous125176940
2050724235072424AG15GENICheterozygous125221589
2050724645072465AG5GENICheterozygous125210332
2050725045072505AG8GENICheterozygous125176941
2050725065072507GA4GENIChomozygous125221590
2050725545072555AG12GENIChomozygous125176942
2050725695072570GC4GENIChomozygous125176943
2050728895072890TA14GENIChomozygous125176944
2050729965072997TA7GENIChomozygous125176945
2050730015073002GA6GENIChomozygous125176946
2050730085073009GA6GENIChomozygous125210336
2050730105073011TG6GENIChomozygous125210337
2050734405073441AG17GENIChomozygous125176947
2050735125073513AG11GENIChomozygous125176948
2050738645073865CT10GENIChomozygous125176949
2050743655074366CA10GENIChomozygous125176950
2050743875074388GC5GENICheterozygous125221591
2050745105074511CT28GENIChomozygous125176953
2050746045074605TC20GENIChomozygous125200181
2050750565075057CA15GENIChomozygous125176954
2050750635075064CT17GENIChomozygous125176955
2050754495075450CT22GENIChomozygous125221592
2050756815075682TC12GENIChomozygous125176956
2050756965075697GA7GENIChomozygous125221593
2050758965075897CT17GENIChomozygous125176957
2050759065075907CT20GENIChomozygous125176958
2050762805076281TC20GENIChomozygous125176959
2050763525076353TC14GENIChomozygous125176960
2050763875076388AG12GENIChomozygous125176961
2050765075076508TC14GENIChomozygous125176963
2050765415076542CT18GENIChomozygous125221594