chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052277117052278AT16GENIChomozygous817936178
8117052890117052891AG19GENIChomozygous817936179
8117053035117053036AG21GENIChomozygous817936180
8117054122117054123CT7GENIChomozygous817936181
8117054158117054159AG7GENIChomozygous817936182
8117055010117055011AG9GENIChomozygous817936183
8117055014117055015AC9GENIChomozygous817936184
8117055369117055370TC18GENIChomozygous817936185
8117055623117055624AC14GENIChomozygous817936186
8117055685117055686CT14GENIChomozygous817936187
8117056118117056119GGA18GENIChomozygous817936188
8117056327117056328CA24GENIChomozygous817936189
8117056459117056460GA8GENIChomozygous817936190
8117057218117057219T-15GENIChomozygous817936191
8117058388117058389AG13GENIChomozygous817936192
8117059204117059205AC12GENIChomozygous817936193
8117060015117060016GA12GENIChomozygous817936194
8117060807117060808CT8GENIChomozygous817936195
8117061256117061257CT8GENIChomozygous817936196
8117061986117061987CT20GENIChomozygous817936197
8117062214117062215CT22GENIChomozygous817936198
8117062340117062341TTGTCA21GENIChomozygous817936199
8117062839117062840CG12GENIChomozygous817936200
8117063514117063515CT16GENIChomozygous817936201
8117063641117063642GC11GENIChomozygous817936202
8117063787117063788TC13GENIChomozygous817936203
8117067190117067191GGCTGT15GENIChomozygous817936204
8117067250117067251AG12GENIChomozygous817936205
8117067587117067588TC18GENIChomozygous817936206
8117068510117068511AG15GENIChomozygous817936207
8117068570117068571TC10GENIChomozygous817936208
8117068680117068681CA13GENIChomozygous817936209
8117068800117068801AG9GENIChomozygous817936210
8117068936117068937TTTC15GENIChomozygous817936211
8117069221117069222GA8GENIChomozygous817936212
8117069252117069253CG10GENIChomozygous817936213
8117070028117070029TC24GENIChomozygous817936214
8117070774117070775TA19GENIChomozygous817936215
8117072502117072503TC13GENIChomozygous817936216
8117074996117074997AG9GENIChomozygous817936217