chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1569546215695463GGAA8GENICpossibly homozygous45097276
X1569547915695480A-11GENIChomozygous45097277
X1569637915696380GA6GENIChomozygous45273859
X1569747315697474GA8GENIChomozygous45097279
X1569749715697498GA10GENIChomozygous45097280
X1569957115699572CT5GENIChomozygous45097281
X1569958215699583CG6GENIChomozygous45097282
X1569992915699930GA13GENIChomozygous45273860
X1570163315701634CT15GENIChomozygous45097284
X1570190615701907TC12GENIChomozygous45097286
X1570209415702096TT--4GENIChomozygous45252066
X1570210715702109TC--6GENICheterozygous45252067
X1570331315703314GGTTTTTTT3GENIChomozygous45273861
X1570393115703932TC12GENIChomozygous45097288
X1570475715704758GA6GENICheterozygous45273862
X1570476215704763AT4GENICheterozygous45273863
X1570479515704796TG5GENIChomozygous45273864
X1570600715706008GA12GENICheterozygous45097289
X1570608615706087TC13GENICheterozygous45097290
X1570808615708087CT7GENIChomozygous45097291
X1570886415708865GA8GENIChomozygous45097292