chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X3747548237475483GT7GENIChomozygous108256567
X3747551537475516AT8GENIChomozygous108256569
X3747568137475682GA3GENIChomozygous108256571
X3747590737475908CA2GENIChomozygous108380360
X3747603637476037CA3GENIChomozygous108256573
X3748968937489690TC5GENIChomozygous108256575
X3749523937495240GT12GENIChomozygous108256577
X3750740237507403CT11GENIChomozygous108256579
X3750748437507485GT8GENIChomozygous108256581
X3750757237507573AG13GENIChomozygous108256583
X3750777937507780GA6GENIChomozygous119916596
X3750882037508821AT9GENIChomozygous119916597
X3754293037542931GA40GENICheterozygous119916598
X3754297237542973AT49GENICheterozygous119916599
X3754297937542980GA48GENICheterozygous119916600
X3755831037558311GA30GENICheterozygous119916601
X3755836937558370AG41GENICheterozygous119916602
X3755841337558414GA32GENICheterozygous119916603
X3755841637558417GA32GENICheterozygous119916604
X3755842137558422TC32GENICheterozygous119916605
X3756069437560695GA58GENICheterozygous119916606
X3756078337560784GT30GENICheterozygous119916607