chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143449330143449330CCCACCCAACTT34GENIChomozygous128531168
7143449516143449517AG47GENIChomozygous115943826
7143449556143449556AAAGG44GENIChomozygous128531169
7143450459143450460AG31GENIChomozygous115943828
7143451043143451044GA36GENIChomozygous116305462
7143451053143451054CT35GENIChomozygous115943829
7143451163143451163G32GENIChomozygous132112925
7143451247143451248AG43GENIChomozygous116305463
7143451267143451268TC44GENICpossibly homozygous116305464
7143451570143451571AG36GENIChomozygous115943831
7143451692143451693CT38GENIChomozygous115943832
7143451775143451776GA46GENIChomozygous116305465
7143452055143452056TG32GENIChomozygous115943833
7143452243143452245TA45GENIChomozygous132112926
7143452688143452689TC44GENIChomozygous115943834
7143452689143452690GA44GENIChomozygous116305466
7143452999143453000GA31GENIChomozygous116305467
7143453338143453339CT36GENIChomozygous116305468