chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9113516238113516239AG22GENIChomozygous117645375
9113518181113518182CT20GENIChomozygous117645376
9113521195113521196CG24GENIChomozygous117645378
9113521297113521298GT19GENIChomozygous117645379
9113523335113523336AC35GENIChomozygous117645380
9113524732113524733AG27GENIChomozygous117645381
9113525384113525385CT25GENIChomozygous117645382
9113525427113525428CT27GENIChomozygous117645383
9113529792113529793TG29GENIChomozygous117742855
9113530116113530117CT22GENIChomozygous117645384
9113532071113532072AG22GENIChomozygous117645385
9113535283113535284CG17GENIChomozygous117645386
9113535761113535762GA24GENIChomozygous117645387
9113537492113537493CT35GENIChomozygous117645388
9113545264113545265GA27GENIChomozygous117645389
9113545784113545785TC34GENIChomozygous117645390
9113546255113546256CT33GENIChomozygous117645391
9113550562113550563CT29GENIChomozygous117645392
9113551212113551213CT26GENIChomozygous117645393
9113552709113552710AG32GENICpossibly homozygous117645394
9113552771113552772TC33GENIChomozygous117645395
9113553145113553146AT39GENIChomozygous117742857
9113553158113553159TC37GENIChomozygous117427185
9113553168113553169CT42GENIChomozygous117645396
9113553528113553529GT16GENICpossibly homozygous117645397
9113554020113554021AG37GENIChomozygous117645398
9113556028113556029CG33GENIChomozygous117645399
9113556081113556082GC30GENIChomozygous117645400
9113556268113556269AG25GENIChomozygous117645401
9113556873113556874CT21GENIChomozygous117645402
9113558300113558301CT24GENIChomozygous117645403
9113559203113559204TC29GENIChomozygous117645404
9113560560113560561GA23GENIChomozygous117427196
9113563038113563039TC34GENIChomozygous117645405
9113567632113567633AC34GENIChomozygous117645406
9113567661113567662GT31GENIChomozygous117645407
9113569775113569776TC37GENIChomozygous117645408
9113570513113570514GT46GENICpossibly homozygous117645409
9113571321113571322TC36GENIChomozygous117427204
9113572457113572458TC31GENIChomozygous117645410