chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109803424109803425AG5GENIChomozygous116719121
10109805182109805183GA10GENIChomozygous116909769
10109805336109805337TC9GENIChomozygous116719123
10109806708109806709TC9GENIChomozygous116719125
10109806825109806826GA15GENIChomozygous116719127
10109807251109807252CG11GENIChomozygous116909770
10109808018109808019AG15GENIChomozygous116719129
10109808148109808149AT4GENIChomozygous116719131
10109808369109808370TC14GENIChomozygous116719133
10109809128109809129CT12GENIChomozygous116719135
10109809149109809150TC12GENIChomozygous116719137
10109809226109809226T13GENIChomozygous128860726
10109809559109809560CA13GENIChomozygous116719139
10109810385109810386AG8GENIChomozygous116719141
10109810682109810683TC7GENIChomozygous116719143
10109809289109809289TGTGTGCA14GENIChomozygous132148075