chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191066861710668618CA26GENIChomozygous46059687
191066919910669200GGGA23GENIChomozygous46059688
191066954910669550CCAAGGCTGGAGACTGGG30GENIChomozygous46059689
191066970510669706TC30GENIChomozygous46059690
191067007210670073AG23GENIChomozygous46788895
191067022810670229TTTCTGTGTGTGTG3GENIChomozygous46788897
191067060010670601TG38GENICpossibly homozygous46059693
191067073210670733TG19GENIChomozygous46059694
191067090410670905AG16GENIChomozygous46059695
191067127010671271T-15GENIChomozygous46059696
191067135510671356CT12GENIChomozygous46546797
191067214810672149AG20GENICpossibly homozygous46059699
191067255610672560GGAG----8GENICpossibly homozygous46397446
191067256110672613GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGGAGGGAGGGAGG----------------------------------------------------10GENICheterozygous46397448
191067332810673329T-34GENIChomozygous46788899
191067356210673563CT28GENIChomozygous46059704
191067421210674213TC38GENIChomozygous46059705
191067474210674743AG17GENIChomozygous46059706
191067477810674779TC16GENIChomozygous46059707
191067490510674906CT23GENIChomozygous46486236
191067255510672567GGGAGAGAGAGA------------8GENICheterozygous46458634
191067050410670505CCTTTTTTTT2GENIChomozygous46428089