chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
82808002128080022AG21GENIChomozygous117099619
82808789028087891AG19GENIChomozygous117099620
82809188428091885TC17GENIChomozygous117099621
82809294928092950GA23GENIChomozygous117099622
82809419428094195AG22GENIChomozygous117099623
82809482928094830GT2GENIChomozygous118077030
82809557228095573GT14GENIChomozygous117099624
82809757228097573TA13GENIChomozygous117099625
82809887228098873TG23GENIChomozygous117099626
82810261828102619AT32GENIChomozygous117099627
82810502928105030TC38GENIChomozygous117099628
82811015028110151GA24GENICpossibly homozygous117099631
82811165728111658TG31GENIChomozygous117099632
82811375628113757AG27GENIChomozygous117099633
82811455728114558CG23GENIChomozygous117099634
82811510828115109GT17GENIChomozygous117099635
82811788128117882GA25GENIChomozygous117099636
82811900728119008TC32GENIChomozygous117099638
82811905228119053AG30GENIChomozygous117099639
82812539428125395AG20GENIChomozygous117099640
82812836328128364CT13GENIChomozygous117099641
82813051628130517AC15GENIChomozygous116443093
82813207428132075GA18GENIChomozygous117099642
82814468728144688CT24GENIChomozygous117099648
82814479928144800CT33GENIChomozygous117099649
82814496828144969GT39GENIChomozygous117099650