chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262264170262265CCA26GENIChomozygous60940238
1170262755170262756CT28GENIChomozygous60940239
1170262801170262802AC40GENIChomozygous60940240
1170263138170263139TA40GENIChomozygous60940241
1170263194170263195TC36GENICpossibly homozygous61908940
1170263253170263254AG26GENIChomozygous60940242
1170263352170263353GA40GENIChomozygous60940244
1170264133170264134AG30GENIChomozygous60940245
1170264186170264187AG25GENIChomozygous60940246
1170264222170264223GGGTTT23GENIChomozygous60940247
1170264757170264758CT30GENIChomozygous60940248
1170265057170265058GA26GENIChomozygous60940250
1170266219170266220CA29GENIChomozygous62271049
1170266220170266221AT29GENIChomozygous62271050
1170266424170266425GA13GENIChomozygous62642022
1170266888170266889CT26GENIChomozygous61908941
1170266926170266927GC23GENIChomozygous60940251
1170267007170267008CT25GENIChomozygous60940252
1170267037170267038GA21GENIChomozygous60940253
1170267149170267150TC20GENIChomozygous60940254
1170267323170267324TC19GENIChomozygous60940256
1170267579170267580GA34GENIChomozygous60940257
1170267593170267594TC33GENIChomozygous60940258
1170267799170267800TC30GENIChomozygous61908942
1170267843170267844AT28GENIChomozygous61908943
1170267958170267959TC26GENIChomozygous60940259
1170268200170268201CT27GENIChomozygous61908944
1170268248170268249GT24GENIChomozygous60940260
1170269050170269051AC19GENICpossibly homozygous60940262
1170269357170269358AG35GENIChomozygous60940263
1170269412170269413AG30GENIChomozygous60940264
1170269505170269506GA23GENIChomozygous61908945
1170270084170270085AAGT10GENICpossibly homozygous62271051
1170270337170270338GA16GENIChomozygous60940267
1170271167170271168TC28GENIChomozygous60940269
1170271631170271632GA35GENIChomozygous60940270
1170271934170271935AG31GENIChomozygous60940271
1170272091170272102AAAAAAAAAAA-----------26GENIChomozygous60940272