chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104657217846572179GT20GENIChomozygous116586254
104657223346572234TC14GENIChomozygous116586256
104657295446572955GA20GENIChomozygous116586258
104657390346573904AG21GENIChomozygous116586260
104657429146574292AG15GENIChomozygous116586262
104657438646574387CA23GENIChomozygous116586264
104657511746575118CT14GENIChomozygous116586266
104657720646577207AC17GENIChomozygous116586268
104657730046577301GA11GENIChomozygous116586270
104657784946577850CA30GENIChomozygous116586272
104657795446577955TG16GENIChomozygous116586274
104657876646578767AG17GENIChomozygous116586276
104658075046580751TC15GENIChomozygous116586278
104658259446582595AT8GENIChomozygous116586280
104658335246583353AG18GENIChomozygous116586286
104658348046583481AG20GENICpossibly homozygous116586288
104658416346584164GA29GENIChomozygous116586290
104658447046584471AG12GENIChomozygous116586292
104658478646584787AT16GENIChomozygous116586294
104658538946585390TC28GENIChomozygous116586296
104658546046585461GA29GENIChomozygous116586298
104658641646586417TC12GENIChomozygous116586300
104658646946586470AG11GENIChomozygous116586302
104658755946587560AT22GENIChomozygous116586304
104658765346587654CA12GENIChomozygous116586306
104658790246587903CT17GENIChomozygous116586308
104658963346589634TG17GENIChomozygous116586310
104658970446589705GT26GENIChomozygous116586312
104659168146591682AC23GENIChomozygous116586314
104659220446592205GA13GENIChomozygous116586316