chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262264170262265CCA36GENIChomozygous60940238
1170262755170262756CT28GENIChomozygous60940239
1170262801170262802AC29GENIChomozygous60940240
1170263138170263139TA27GENIChomozygous60940241
1170263253170263254AG37GENIChomozygous60940242
1170263352170263353GA30GENIChomozygous60940244
1170264133170264134AG30GENIChomozygous60940245
1170264186170264187AG32GENIChomozygous60940246
1170264222170264223GGGTTT20GENIChomozygous60940247
1170264757170264758CT25GENIChomozygous60940248
1170265057170265058GA29GENIChomozygous60940250
1170266219170266220CA34GENIChomozygous62271049
1170266220170266221AT35GENIChomozygous62271050
1170266888170266889CT23GENIChomozygous61908941
1170266926170266927GC26GENIChomozygous60940251
1170267007170267008CT29GENIChomozygous60940252
1170267037170267038GA31GENIChomozygous60940253
1170267149170267150TC32GENIChomozygous60940254
1170267323170267324TC30GENIChomozygous60940256
1170267579170267580GA29GENIChomozygous60940257
1170267593170267594TC27GENIChomozygous60940258
1170267799170267800TC26GENIChomozygous61908942
1170267843170267844AT30GENIChomozygous61908943
1170267958170267959TC25GENIChomozygous60940259
1170268200170268201CT28GENIChomozygous61908944
1170268248170268249GT21GENIChomozygous60940260
1170269050170269051AC20GENIChomozygous60940262
1170269357170269358AG28GENIChomozygous60940263
1170269412170269413AG30GENIChomozygous60940264
1170269505170269506GA28GENIChomozygous61908945
1170270084170270085AAGT15GENICpossibly homozygous62271051
1170270337170270338GA25GENIChomozygous60940267
1170271167170271168TC20GENIChomozygous60940269
1170271631170271632GA24GENIChomozygous60940270
1170271934170271935AG26GENIChomozygous60940271
1170272091170272102AAAAAAAAAAA-----------20GENIChomozygous60940272