chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262264170262265CCA29GENIChomozygous60940238
1170262755170262756CT27GENIChomozygous60940239
1170262801170262802AC33GENIChomozygous60940240
1170263138170263139TA28GENIChomozygous60940241
1170263194170263195TC45GENIChomozygous61908940
1170263253170263254AG34GENIChomozygous60940242
1170263352170263353GA39GENIChomozygous60940244
1170264133170264134AG34GENIChomozygous60940245
1170264186170264187AG30GENIChomozygous60940246
1170264222170264223GGGTTT18GENIChomozygous60940247
1170264757170264758CT30GENIChomozygous60940248
1170265057170265058GA27GENIChomozygous60940250
1170266888170266889CT39GENIChomozygous61908941
1170266926170266927GC35GENIChomozygous60940251
1170267007170267008CT40GENIChomozygous60940252
1170267037170267038GA38GENIChomozygous60940253
1170267149170267150TC35GENIChomozygous60940254
1170267323170267324TC35GENIChomozygous60940256
1170267579170267580GA39GENIChomozygous60940257
1170267593170267594TC36GENIChomozygous60940258
1170267799170267800TC44GENIChomozygous61908942
1170267843170267844AT33GENIChomozygous61908943
1170267958170267959TC37GENIChomozygous60940259
1170266219170266220CA22GENIChomozygous62271049
1170266220170266221AT22GENIChomozygous62271050
1170268200170268201CT28GENIChomozygous61908944
1170268248170268249GT31GENIChomozygous60940260
1170269050170269051AC25GENIChomozygous60940262
1170269357170269358AG39GENIChomozygous60940263
1170269412170269413AG32GENIChomozygous60940264
1170269505170269506GA47GENIChomozygous61908945
1170270337170270338GA39GENIChomozygous60940267
1170271167170271168TC39GENIChomozygous60940269
1170271631170271632GA43GENIChomozygous60940270
1170271934170271935AG19GENIChomozygous60940271
1170272091170272102AAAAAAAAAAA-----------26GENIChomozygous60940272