chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46856957068569571GA64GENIChomozygous112691587
46857027568570276AG64GENIChomozygous112691589
46857128068571281AG54GENIChomozygous112691591
46857142268571423TC54GENIChomozygous112691593
46857193368571934CT48GENIChomozygous113347162
46857234968572350GA57GENIChomozygous112691597
46857236668572367GA52GENICheterozygous113347163
46857237068572371GA52GENICheterozygous113347165
46857371668573717GA21GENIChomozygous112691599
46857397968573980TA61GENICheterozygous112691601
46857470268574703CT30GENIChomozygous112691603
46857579768575798GA31GENIChomozygous112691605
46857751768577518AG51GENIChomozygous112691607
46857766868577669TC65GENIChomozygous112691609
46857808468578085GA60GENIChomozygous112691611
46857927268579273GA51GENIChomozygous112691613
46857951868579519AG53GENICpossibly homozygous112691615
46858057768580578CT47GENIChomozygous112691617
46858124168581242TA54GENIChomozygous112691619
46858274268582743CG45GENIChomozygous112691621
46858354968583550TC49GENIChomozygous112691623
46858361868583619CT43GENICpossibly homozygous112691625
46858568468585685TC37GENIChomozygous112691627
46858795168587952AG40GENIChomozygous112691629
46858838568588386TA35GENIChomozygous112691631
46859278668592787TC66GENIChomozygous112691633
46859582468595825CA38GENICheterozygous113511974