chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1569546215695463GGAA7GENIChomozygous45097276
X1569547915695480A-7GENIChomozygous45097277
X1569565915695660CT18GENIChomozygous45097278
X1569747315697474GA14GENIChomozygous45097279
X1569749715697498GA15GENIChomozygous45097280
X1569957115699572CT11GENIChomozygous45097281
X1569958215699583CG12GENIChomozygous45097282
X1570099615700997TC11GENICheterozygous45097283
X1570163315701634CT22GENIChomozygous45097284
X1570165315701654CT25GENIChomozygous45097285
X1570190615701907TC7GENIChomozygous45097286
X1570209515702098TTT---9GENICheterozygous45647138
X1570209715702098T-9GENICheterozygous45501147
X1570393115703932TC11GENIChomozygous45097288
X1570600715706008GA18GENICpossibly homozygous45097289
X1570605115706054TTC---6GENICheterozygous45501151
X1570886415708865GA7GENIChomozygous45097292