chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262264170262265CCA38GENICpossibly homozygous60940238
1170262755170262756CT20GENIChomozygous60940239
1170262801170262802AC28GENIChomozygous60940240
1170263138170263139TA33GENIChomozygous60940241
1170263253170263254AG33GENIChomozygous60940242
1170263352170263353GA31GENIChomozygous60940244
1170264133170264134AG21GENIChomozygous60940245
1170264186170264187AG23GENIChomozygous60940246
1170264222170264223GGGTTT21GENIChomozygous60940247
1170264757170264758CT29GENIChomozygous60940248
1170265057170265058GA27GENIChomozygous60940250
1170266219170266220CA15GENIChomozygous62271049
1170266220170266221AT15GENIChomozygous62271050
1170266888170266889CT17GENIChomozygous61908941
1170266926170266927GC19GENIChomozygous60940251
1170267007170267008CT24GENIChomozygous60940252
1170267037170267038GA20GENIChomozygous60940253
1170267149170267150TC20GENIChomozygous60940254
1170267323170267324TC31GENIChomozygous60940256
1170267579170267580GA32GENIChomozygous60940257
1170267593170267594TC31GENIChomozygous60940258
1170267799170267800TC32GENIChomozygous61908942
1170267843170267844AT35GENIChomozygous61908943
1170267958170267959TC31GENIChomozygous60940259
1170268200170268201CT29GENIChomozygous61908944
1170268248170268249GT35GENIChomozygous60940260
1170269050170269051AC25GENIChomozygous60940262
1170269357170269358AG20GENIChomozygous60940263
1170269412170269413AG23GENIChomozygous60940264
1170269505170269506GA22GENIChomozygous61908945
1170270084170270085AAGT7GENIChomozygous62271051
1170270337170270338GA26GENIChomozygous60940267
1170271167170271168TC26GENIChomozygous60940269
1170271631170271632GA22GENIChomozygous60940270
1170271934170271935AG26GENIChomozygous60940271
1170272091170272102AAAAAAAAAAA-----------28GENIChomozygous60940272