chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1569957115699572CT6GENIChomozygous45097281
X1569958215699583CG5GENIChomozygous45097282
X1570099615700997TC11GENIChomozygous45097283
X1570163315701634CT9GENIChomozygous45097284
X1570165315701654CT7GENIChomozygous45097285
X1570190615701907TC11GENIChomozygous45097286
X1570393115703932TC7GENIChomozygous45097288
X1570600715706008GA5GENIChomozygous45097289
X1570209715702098T-11GENICpossibly homozygous45501147
X1570331315703314GGTTTT7GENICheterozygous45501149
X1570331315703314GGTTTTT7GENICheterozygous45585110