chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89015165090151651CT13GENIChomozygous52719162
89015193190151932TTAGAG23GENIChomozygous52719165
89015259490152595CT14GENIChomozygous52719168
89015415390154154GA11GENIChomozygous52719179
89015267890152685TACCATG-------8GENIChomozygous52719171
89015304190153042TG19GENIChomozygous52719174
89015401290154013CT11GENIChomozygous52719177
89015480990154810CT12GENIChomozygous52719182
89015481190154812CA12GENIChomozygous52719185
89015491190154912A-10GENIChomozygous54261028
89015547690155477GT12GENIChomozygous52719189
89015560090155601GT14GENIChomozygous52719192
89015587490155875GGC14GENIChomozygous52719196
89015601090156011AG18GENIChomozygous52719199
89015605190156052CT21GENIChomozygous52719202
89015666190156662CA15GENIChomozygous52719204
89015685590156856AG16GENIChomozygous52719206
89015720090157201CT22GENIChomozygous52719209
89015722590157226TA19GENIChomozygous52719212
89015776290157763CT16GENIChomozygous52719216
89015807490158075AG22GENIChomozygous52719219
89015828390158284AC15GENIChomozygous52719221
89015855790158558CT16GENIChomozygous52719224
89015915990159160GA19GENIChomozygous52719227
89015923890159239TC18GENIChomozygous52719235
89015928290159283CA20GENIChomozygous52719238
89015934190159342CT22GENIChomozygous52719240
89017170490171705A-13GENIChomozygous52719279
89017171690171717C-15GENIChomozygous52719281
89017173790171738C-11GENIChomozygous52719284
89017174890171749G-12GENIChomozygous52719287
89018262890182629A-15GENIChomozygous52719306
89018264990182650TC18GENIChomozygous52719308
89018528990185290TA17GENIChomozygous52719322
89018631790186318GC12GENIChomozygous54335836
89018391590183916GC19GENIChomozygous53220063
89018394390183944CA21GENICpossibly homozygous53220064