chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1569957115699572CT6GENIChomozygous45097281
X1569958215699583CG5GENIChomozygous45097282
X1570099615700997TC9GENICpossibly homozygous45097283
X1570165315701654CT6GENICheterozygous45097285
X1570190615701907TC11GENIChomozygous45097286
X1570209715702098T-2GENICheterozygous45501147
X1570393115703932TC10GENIChomozygous45097288