chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109796903397969034GA37GENIChomozygous116828051
109797036097970361CT39GENIChomozygous116695462
109798305597983056TC24GENIChomozygous116695534
109800179298001793GC16GENIChomozygous116695660
109800181398001814AG14GENIChomozygous116828053
109800224598002246AC18GENIChomozygous116828055
109800226998002270CA18GENIChomozygous116828057
109800729798007298CT33GENIChomozygous116828059
109801043198010432AC36GENIChomozygous116695672
109801325698013257TC34GENIChomozygous116695678
109801373698013737AG28GENIChomozygous116695680
109801391798013918TC25GENIChomozygous116828061
109801421498014215TC16GENIChomozygous116828063
109801524798015248GA27GENIChomozygous116695682
109801526198015262CT26GENIChomozygous116695684
109801543398015434AG29GENIChomozygous116695688
109801575198015752TC32GENIChomozygous116828065
109801644698016447AG49GENIChomozygous116828067
109801660298016603GT40GENIChomozygous116695690