chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6101408781101408782GT18GENIChomozygous114918515
6101409833101409834GA30GENIChomozygous114918516
6101410137101410138TC24GENIChomozygous114918517
6101410480101410481GC20GENIChomozygous114918518
6101410571101410572AG28GENIChomozygous115142974
6101410576101410577AG24GENIChomozygous114918520
6101410582101410583TC25GENIChomozygous114918521
6101410583101410584AG25GENIChomozygous114918522
6101410584101410585AC26GENIChomozygous114918523
6101410598101410599AG29GENIChomozygous118619499
6101410619101410620AC34GENIChomozygous114918524
6101410853101410854AC27GENIChomozygous114918525