chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191066861710668618CA23GENIChomozygous46059687
191066919910669200GGGA22GENIChomozygous46059688
191066954910669550CCAAGGCTGGAGACTGGG30GENIChomozygous46059689
191066970510669706TC26GENIChomozygous46059690
191066997710669978GA14GENIChomozygous46059691
191067023210670233GGTGTGTGTGTC10GENICheterozygous46458632
191067023410670235GGTGTGTGTC10GENICheterozygous46507218
191067050410670505CCTTTTTTTT7GENIChomozygous46428089
191067060010670601TG15GENIChomozygous46059693
191067073210670733TG9GENIChomozygous46059694
191067090410670905AG8GENIChomozygous46059695
191067127010671271T-16GENIChomozygous46059696
191067132410671325TC10GENIChomozygous46059697
191067199510671996CT22GENIChomozygous46059698
191067214810672149AG15GENIChomozygous46059699
191067255510672567GGGAGAGAGAGA------------6GENICheterozygous46458634
191067255610672560GGAG----6GENICheterozygous46397446
191067256110672613GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGGAGGGAGGGAGG----------------------------------------------------10GENICheterozygous46397448
191067259410672595A-4GENICheterozygous46507221
191067259610672597AG3GENICheterozygous46507223
191067259810672599AG4GENICheterozygous46507225
191067271710672718CT11GENIChomozygous46059702
191067356210673563CT17GENIChomozygous46059704
191067421210674213TC28GENIChomozygous46059705
191067474210674743AG18GENIChomozygous46059706
191067477810674779TC18GENIChomozygous46059707