chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262264170262265CCA26GENIChomozygous60940238
1170262755170262756CT24GENIChomozygous60940239
1170262801170262802AC32GENIChomozygous60940240
1170263138170263139TA31GENIChomozygous60940241
1170263194170263195TC34GENIChomozygous61908940
1170263253170263254AG27GENIChomozygous60940242
1170263352170263353GA27GENIChomozygous60940244
1170264133170264134AG22GENIChomozygous60940245
1170264186170264187AG31GENIChomozygous60940246
1170264222170264223GGGTTT30GENIChomozygous60940247
1170264757170264758CT26GENIChomozygous60940248
1170265057170265058GA36GENIChomozygous60940250
1170266888170266889CT17GENIChomozygous61908941
1170266926170266927GC19GENIChomozygous60940251
1170267007170267008CT39GENIChomozygous60940252
1170267037170267038GA28GENIChomozygous60940253
1170267149170267150TC25GENIChomozygous60940254
1170267323170267324TC19GENIChomozygous60940256
1170267579170267580GA33GENIChomozygous60940257
1170267593170267594TC29GENIChomozygous60940258
1170267799170267800TC22GENIChomozygous61908942
1170267843170267844AT28GENIChomozygous61908943
1170267958170267959TC27GENIChomozygous60940259
1170268200170268201CT29GENIChomozygous61908944
1170268248170268249GT22GENIChomozygous60940260
1170269050170269051AC29GENIChomozygous60940262
1170269357170269358AG23GENIChomozygous60940263
1170269412170269413AG24GENIChomozygous60940264
1170269505170269506GA25GENIChomozygous61908945
1170270337170270338GA20GENIChomozygous60940267
1170271167170271168TC21GENIChomozygous60940269
1170271631170271632GA35GENIChomozygous60940270
1170271934170271935AG18GENIChomozygous60940271
1170272091170272102AAAAAAAAAAA-----------14GENIChomozygous60940272
1170266219170266220CA25GENIChomozygous62271049
1170266220170266221AT25GENIChomozygous62271050
1170270084170270085AAGT7GENIChomozygous62271051