chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181577968115779682A52GENIChomozygous140211571
181577969815779699AG53GENIChomozygous140271427
181577982015779821AT52GENIChomozygous142640671
181577985915779860GC52GENIChomozygous140271428
181578009215780093TG48GENIChomozygous140271430
181578064215780643TC39GENIChomozygous140271431
181578117515781176AG58GENIChomozygous140271432
181578185915781860AG51GENIChomozygous140271434
181578261015782611TA65GENIChomozygous140271436
181578261915782620AT65GENIChomozygous140271437
181578379615783797CT38GENIChomozygous140271439
181578471715784718GA56GENIChomozygous140271440
181578476615784767AT51GENIChomozygous140271441
181578561215785613GA58GENICpossibly homozygous140271442
181578593415785935GA62GENIChomozygous140271443
181578622515786226CT53GENIChomozygous140271445
181578111515781115GGGAAGGA40GENIChomozygous142628144
181578654315786544AG60GENIChomozygous140271446
181578379615783797C38GENICheterozygous403430196