chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219126734219126735GA21GENIChomozygous108540265
1219127453219127454AG8GENIChomozygous108540267
1219128940219128941AG28GENIChomozygous108540274
1219129397219129398CT16GENIChomozygous108540276
1219130812219130813CT18GENIChomozygous108540278
1219130821219130822TC19GENIChomozygous108540280
1219132337219132341GGAA11GENIChomozygous127484463
1219132402219132403CT14GENIChomozygous108540281
1219133301219133302CG16GENIChomozygous108540283
1219134090219134091GC23GENIChomozygous108540285
1219135248219135249G16GENIChomozygous127484464
1219136402219136403GA24GENIChomozygous108540287
1219136949219136950TC15GENIChomozygous108540289
1219137029219137043CCTGATGTGGGTTA17GENIChomozygous131992299
1219137648219137649CA10GENIChomozygous108540291
1219138083219138084AG18GENIChomozygous108540292
1219138412219138429ACACCCCTCCCCCCAAT20GENIChomozygous127484465
1219138430219138432CC20GENIChomozygous127484466
1219138434219138445GTGGACACCCC20GENIChomozygous127484467