chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8119113000119113001CT30GENIChomozygous116676263
8119113196119113197CA28GENIChomozygous116676265
8119113925119113926AT21GENIChomozygous116676267
8119114457119114458GT30GENIChomozygous116676269
8119114627119114628TG19GENIChomozygous116676271
8119114650119114651CT22GENIChomozygous116676273
8119114962119114963GA31GENIChomozygous116676275
8119115577119115578GA23GENIChomozygous116676277
8119115675119115676TC30GENIChomozygous116676279
8119116192119116193TC32GENIChomozygous116676283
8119116278119116279CT34GENIChomozygous116676285
8119116355119116356CT37GENIChomozygous117062539
8119117155119117156CA22GENIChomozygous118077663
8119117159119117160CA25GENIChomozygous117174185
8119117543119117544AG36GENIChomozygous116676291
8119117872119117873TC26GENICpossibly homozygous116676293
8119118160119118161GA35GENIChomozygous116676295