chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109064511590645116TA16GENIChomozygous117087889
109064690090646901AG22GENIChomozygous116676811
109064751190647512GA16GENIChomozygous116951506
109064858790648588GT6GENIChomozygous116951508
109065069790650698TA19GENIChomozygous116676815
109065209590652096TC2GENIChomozygous116676817
109065411790654118AG25GENIChomozygous116951512
109065512390655124TC19GENIChomozygous117228001
109065530490655305CT17GENIChomozygous116676821
109065561490655615CG19GENIChomozygous116676823
109065608190656082AT30GENIChomozygous116676825
109065636990656370GT16GENIChomozygous116676827
109065707190657072AG11GENIChomozygous116676829
109065707290657073CT10GENIChomozygous116676831
109065765690657657AG18GENIChomozygous116676833
109065785090657851GT13GENIChomozygous116676835
109065800490658005AG13GENIChomozygous116676837