chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1177592120177592121GT18GENIChomozygous109524882
1177592337177592338CT17GENIChomozygous109524883
1177592368177592369CT16GENIChomozygous109524884
1177592437177592438TC11GENIChomozygous109524885
1177593053177593054CT22GENIChomozygous109524886
1177594262177594263CA14GENIChomozygous109524887