chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X123900994123900995AG16GENIChomozygous936924382
X123901333123901334TC16GENIChomozygous936924383
X123901666123901667CA9GENIChomozygous936924384
X123902771123902772CT13GENIChomozygous936924385
X123903040123903041CT11GENIChomozygous936924386
X123903719123903720TA15GENIChomozygous936924387
X123904886123904887AC11GENIChomozygous936924388
X123904966123904967GA6GENIChomozygous936924389
X123905627123905628AG6GENIChomozygous936924390
X123906352123906353GT12GENIChomozygous936924391
X123906808123906809AG14GENIChomozygous936924392
X123906932123906933TA24GENIChomozygous936924393
X123907599123907600CT9GENIChomozygous936924394
X123909136123909137CG11GENIChomozygous936924395
X123911461123911462GT11INTERGENIChomozygous936924396
X123911482123911483GA13INTERGENIChomozygous936924397
X123911483123911484TG12INTERGENIChomozygous936924398
X123912197123912198TC9INTERGENIChomozygous936924399
X123914613123914614AG18INTERGENIChomozygous936924400
X123916196123916197AG13INTERGENIChomozygous936924401
X123916552123916553GA17INTERGENIChomozygous936924402
X123916936123916937AG14INTERGENIChomozygous936924403