chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109803424109803425AG13GENIChomozygous116719121
10109805336109805337TC14GENIChomozygous116719123
10109806708109806709TC17GENIChomozygous116719125
10109806825109806826GA20GENIChomozygous116719127
10109808018109808019AG14GENIChomozygous116719129
10109808148109808149AT19GENIChomozygous116719131
10109808369109808370TC14GENIChomozygous116719133
10109809128109809129CT31GENIChomozygous116719135
10109809149109809150TC27GENIChomozygous116719137
10109809559109809560CA18GENIChomozygous116719139
10109810385109810386AG12GENIChomozygous116719141