chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219126734219126735GA19GENIChomozygous108540265
1219127453219127454AG14GENIChomozygous108540267
1219128461219128462CT16GENIChomozygous108540268
1219128561219128562GA17GENIChomozygous108540270
1219128725219128726CT15GENICheterozygous109367712
1219128940219128941AG21GENIChomozygous108540274
1219129397219129398CT9GENIChomozygous108540276
1219130446219130447GT17GENIChomozygous109367713
1219130812219130813CT9GENIChomozygous108540278
1219130821219130822TC8GENIChomozygous108540280
1219133068219133069CT24GENIChomozygous109367714
1219133301219133302CG13GENIChomozygous108540283
1219134090219134091GC5GENIChomozygous108540285
1219136402219136403GA8GENIChomozygous108540287
1219136949219136950TC13GENIChomozygous108540289
1219136965219136966AG17GENIChomozygous109367715
1219137648219137649CA4GENIChomozygous108540291
1219138083219138084AG14GENIChomozygous108540292
1219138403219138404CG11GENICheterozygous109367717