chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104657217846572179GT35GENIChomozygous116586254
104657223346572234TC38GENIChomozygous116586256
104657295446572955GA37GENIChomozygous116586258
104657390346573904AG33GENIChomozygous116586260
104657429146574292AG40GENIChomozygous116586262
104657438646574387CA27GENIChomozygous116586264
104657511746575118CT29GENIChomozygous116586266
104657720646577207AC33GENIChomozygous116586268
104657730046577301GA22GENIChomozygous116586270
104657784946577850CA41GENIChomozygous116586272
104657795446577955TG45GENIChomozygous116586274
104657876646578767AG33GENIChomozygous116586276
104658075046580751TC41GENIChomozygous116586278
104658121946581220GA8GENIChomozygous117058730
104658259446582595AT32GENIChomozygous116586280
104658259646582597AG30GENIChomozygous116586282
104658308046583081AT11GENIChomozygous116586284
104658316146583162CG7GENIChomozygous116877811
104658335246583353AG30GENIChomozygous116586286
104658348046583481AG28GENIChomozygous116586288
104658416346584164GA27GENIChomozygous116586290
104658447046584471AG35GENIChomozygous116586292
104658478646584787AT26GENIChomozygous116586294
104658488746584888CG36GENIChomozygous117058732
104658538946585390TC34GENIChomozygous116586296
104658546046585461GA41GENIChomozygous116586298
104658641646586417TC16GENIChomozygous116586300
104658646946586470AG25GENIChomozygous116586302
104658755946587560AT34GENIChomozygous116586304
104658765346587654CA40GENIChomozygous116586306
104658790246587903CT32GENIChomozygous116586308
104658963346589634TG30GENIChomozygous116586310
104658970446589705GT31GENIChomozygous116586312
104659168146591682AC26GENIChomozygous116586314
104659220446592205GA28GENIChomozygous116586316
104659282046592821AG32GENIChomozygous116586318