chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219126734219126735GA11GENIChomozygous108540265
1219127453219127454AG23GENIChomozygous108540267
1219128461219128462CT22GENIChomozygous108540268
1219128561219128562GA28GENIChomozygous108540270
1219128739219128740TC38GENIChomozygous108540272
1219128940219128941AG20GENIChomozygous108540274
1219129397219129398CT21GENIChomozygous108540276
1219130812219130813CT31GENICpossibly homozygous108540278
1219130821219130822TC31GENICpossibly homozygous108540280
1219132337219132341GGAA14GENIChomozygous127484463
1219132402219132403CT19GENIChomozygous108540281
1219133301219133302CG23GENIChomozygous108540283
1219134090219134091GC30GENIChomozygous108540285
1219135248219135249G21GENIChomozygous127484464
1219136402219136403GA25GENIChomozygous108540287
1219136949219136950TC27GENIChomozygous108540289
1219137648219137649CA22GENIChomozygous108540291
1219138083219138084AG17GENIChomozygous108540292
1219138412219138429ACACCCCTCCCCCCAAT25GENIChomozygous127484465
1219138430219138432CC25GENIChomozygous127484466
1219138434219138445GTGGACACCCC25GENIChomozygous127484467