chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6146124492146124493CCGTGTGTGTGTGTGTGTGT16GENIChomozygous760912423
6146124694146124695GA29GENIChomozygous656495007
6146125141146125142CT19GENIChomozygous656495008
6146125756146125757A-11GENICpossibly homozygous760912425
6146126532146126533GGGTGTGT9GENICheterozygous760912427
6146127571146127572CT32GENIChomozygous656495009
6146127830146127840GCGTGTGTGA----------13GENICpossibly homozygous760912428
6146127867146127868CCGT7GENICpossibly homozygous760912432
6146127922146127923CA20GENIChomozygous656495010
6146130058146130059AG34GENICpossibly homozygous656495011
6146130178146130179CA30GENICpossibly homozygous656495012