chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1569546215695463GGAA13GENIChomozygous45097276
X1569547915695480A-9GENICpossibly homozygous45097277
X1569565915695660CT23GENIChomozygous45097278
X1569747315697474GA16GENIChomozygous45097279
X1569749715697498GA15GENIChomozygous45097280
X1569957115699572CT9GENIChomozygous45097281
X1569958215699583CG6GENIChomozygous45097282
X1570099615700997TC8GENIChomozygous45097283
X1570163315701634CT19GENIChomozygous45097284
X1570165315701654CT16GENIChomozygous45097285
X1570190615701907TC10GENIChomozygous45097286
X1570209715702098T-5GENICheterozygous45501147
X1570331315703314GGTTTT1GENIChomozygous45501149
X1570393115703932TC18GENIChomozygous45097288
X1570600715706008GA8GENIChomozygous45097289
X1570605115706054TTC---10GENICheterozygous45501151
X1570886415708865GA9GENIChomozygous45097292