chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221470777221470778AG13GENIChomozygous108994885
1221471008221471009CT14GENIChomozygous108994886
1221472393221472394CT5GENIChomozygous108994888
1221472531221472532TA13GENIChomozygous120512305
1221472534221472535AG13GENIChomozygous120475990
1221473064221473065TA15GENIChomozygous108994894
1221473262221473263CT15GENIChomozygous108994895
1221473925221473926GA23GENIChomozygous108994897
1221474631221474632TC25GENIChomozygous108994899
1221474861221474862TC25GENIChomozygous108994900
1221474925221474926GC23GENIChomozygous120490591
1221476859221476860CT19GENIChomozygous108994903
1221477347221477348TC17GENIChomozygous108994904
1221477614221477615AG10GENIChomozygous108994905
1221479154221479155GA20GENIChomozygous108994906
1221480468221480469AG21GENIChomozygous108994907
1221480536221480537AG18GENIChomozygous108994908
1221480605221480606CT16GENIChomozygous108994909
1221482859221482860TC11GENIChomozygous108994911
1221483736221483737CT17GENIChomozygous108994912