chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143449330143449330CCCACCCAACTT25GENIChomozygous128531168
7143449516143449517AG27GENIChomozygous115943826
7143449556143449556AAAGG24GENIChomozygous128531169
7143450459143450460AG21GENIChomozygous115943828
7143451043143451044GA19GENIChomozygous116305462
7143451053143451054CT21GENIChomozygous115943829
7143451247143451248AG36GENIChomozygous116305463
7143451267143451268TC37GENIChomozygous116305464
7143451570143451571AG23GENIChomozygous115943831
7143451692143451693CT26GENIChomozygous115943832
7143451775143451776GA25GENIChomozygous116305465
7143452055143452056TG30GENIChomozygous115943833
7143452688143452689TC34GENIChomozygous115943834
7143452689143452690GA34GENIChomozygous116305466
7143452999143453000GA22GENIChomozygous116305467
7143453338143453339CT18GENIChomozygous116305468
7143451163143451163G26GENIChomozygous132112925
7143452243143452245TA24GENIChomozygous132112926