chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262264170262265CCA26GENIChomozygous60940238
1170262755170262756CT21GENIChomozygous60940239
1170262801170262802AC25GENIChomozygous60940240
1170263138170263139TA22GENIChomozygous60940241
1170263194170263195TC27GENIChomozygous61908940
1170263253170263254AG27GENIChomozygous60940242
1170263352170263353GA23GENIChomozygous60940244
1170264133170264134AG22GENIChomozygous60940245
1170264186170264187AG26GENIChomozygous60940246
1170264222170264223GGGTTT21GENIChomozygous60940247
1170264757170264758CT15GENIChomozygous60940248
1170265057170265058GA18GENIChomozygous60940250
1170266219170266220CA19GENIChomozygous62271049
1170266220170266221AT20GENIChomozygous62271050
1170266888170266889CT27GENIChomozygous61908941
1170266926170266927GC22GENIChomozygous60940251
1170267007170267008CT19GENIChomozygous60940252
1170267037170267038GA24GENIChomozygous60940253
1170267149170267150TC28GENIChomozygous60940254
1170267323170267324TC23GENIChomozygous60940256
1170267579170267580GA29GENIChomozygous60940257
1170267593170267594TC31GENIChomozygous60940258
1170267799170267800TC24GENIChomozygous61908942
1170267843170267844AT27GENIChomozygous61908943
1170267958170267959TC31GENIChomozygous60940259
1170268200170268201CT16GENIChomozygous61908944
1170268248170268249GT22GENIChomozygous60940260
1170269050170269051AC22GENIChomozygous60940262
1170269357170269358AG31GENIChomozygous60940263
1170269412170269413AG23GENIChomozygous60940264
1170269505170269506GA17GENIChomozygous61908945
1170270337170270338GA31GENIChomozygous60940267
1170271167170271168TC15GENIChomozygous60940269
1170271631170271632GA23GENIChomozygous60940270
1170271934170271935AG24GENIChomozygous60940271
1170272091170272102AAAAAAAAAAA-----------14GENIChomozygous60940272