chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1569546215695463GGAA12GENIChomozygous45097276
X1569547915695480A-12GENIChomozygous45097277
X1569565915695660CT11GENIChomozygous45097278
X1569747315697474GA9GENIChomozygous45097279
X1569749715697498GA13GENIChomozygous45097280
X1569957115699572CT13GENIChomozygous45097281
X1569958215699583CG13GENIChomozygous45097282
X1570099615700997TC5GENIChomozygous45097283
X1570163315701634CT13GENIChomozygous45097284
X1570165315701654CT14GENIChomozygous45097285
X1570190615701907TC11GENIChomozygous45097286
X1570331315703314GGTTTTT8GENICpossibly homozygous45585110
X1570393115703932TC8GENIChomozygous45097288
X1570600715706008GA5GENIChomozygous45097289
X1570886415708865GA9GENIChomozygous45097292
X1570209715702098T-6GENIChomozygous45501147
X1570331315703314GGTTTT8GENICheterozygous45501149