chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181577968115779682A16GENIChomozygous140211571
181577969815779699AG15GENIChomozygous140271427
181577985915779860GC26GENIChomozygous140271428
181578009215780093TG19GENIChomozygous140271430
181578064215780643TC27GENIChomozygous140271431
181578111515781115GGGAAGGA16GENIChomozygous142628144
181578117515781176AG21GENIChomozygous140271432
181578185915781860AG15GENIChomozygous140271434
181578229915782301CC14GENIChomozygous144489242
181578261015782611TA21GENIChomozygous140271436
181578261915782620AT19GENIChomozygous140271437
181578379615783797CT14GENIChomozygous140271439
181578471715784718GA19GENIChomozygous140271440
181578476615784767AT13GENIChomozygous140271441
181578561215785613GA19GENIChomozygous140271442
181578591715785917C21GENIChomozygous144489243
181578593415785935GA19GENIChomozygous140271443
181578622515786226CT14GENIChomozygous140271445
181578654315786544AG14GENIChomozygous140271446
181578379615783797C14GENICheterozygous403430196