chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109803424109803425AG28GENIChomozygous116719121
10109805336109805337TC20GENIChomozygous116719123
10109806708109806709TC29GENICpossibly homozygous116719125
10109806825109806826GA33GENICpossibly homozygous116719127
10109808018109808019AG21GENIChomozygous116719129
10109808148109808149AT31GENICpossibly homozygous116719131
10109808369109808370TC30GENIChomozygous116719133
10109809128109809129CT38GENIChomozygous116719135
10109809149109809150TC32GENIChomozygous116719137
10109809559109809560CA27GENIChomozygous116719139
10109810385109810386AG25GENICpossibly homozygous116719141
10109810682109810683TC7GENIChomozygous116719143