chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1569692115696922GC9GENICpossibly homozygous45807362
X1569695015696951TA7GENICpossibly homozygous45807363
X1569747315697474GA14GENIChomozygous45097279
X1569749715697498GA12GENIChomozygous45097280
X1569957115699572CT14GENIChomozygous45097281
X1569958215699583CG15GENIChomozygous45097282
X1570061015700611CG6GENICheterozygous45473719
X1570089915700900GA7GENIChomozygous45807364
X1570097215700973TG9GENIChomozygous45807365
X1570115315701154GT7GENIChomozygous45807366
X1570124315701244C-12GENIChomozygous45473721
X1570190615701907TC10GENIChomozygous45097286
X1570209415702098TTTT----13GENICpossibly homozygous45807367
X1570331315703314GGTT3GENIChomozygous45585108
X1570368015703681GA9GENICpossibly homozygous45807368
X1570393115703932TC11GENIChomozygous45097288
X1570425315704254CT13GENIChomozygous45807369
X1570479515704796TG10GENIChomozygous45273864
X1570479815704799TC10GENICpossibly homozygous45807370
X1570600715706008GA16GENIChomozygous45097289
X1570605115706054TTC---12GENICheterozygous45501151
X1570886415708865GA9GENICheterozygous45097292