chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262264170262265CCA18GENIChomozygous60940238
1170262755170262756CT50GENIChomozygous60940239
1170262801170262802AC35GENIChomozygous60940240
1170263138170263139TA23GENIChomozygous60940241
1170263194170263195TC33GENIChomozygous61908940
1170263253170263254AG34GENIChomozygous60940242
1170263352170263353GA51GENIChomozygous60940244
1170264133170264134AG38GENIChomozygous60940245
1170264186170264187AG30GENIChomozygous60940246
1170264222170264223GGGTTT14GENIChomozygous60940247
1170264757170264758CT22GENIChomozygous60940248
1170265057170265058GA26GENIChomozygous60940250
1170266888170266889CT58GENIChomozygous61908941
1170266926170266927GC55GENIChomozygous60940251
1170267007170267008CT40GENIChomozygous60940252
1170267037170267038GA45GENIChomozygous60940253
1170267149170267150TC54GENIChomozygous60940254
1170267323170267324TC24GENIChomozygous60940256
1170267579170267580GA24GENIChomozygous60940257
1170267593170267594TC24GENIChomozygous60940258
1170267799170267800TC33GENIChomozygous61908942
1170267843170267844AT35GENIChomozygous61908943
1170267958170267959TC34GENIChomozygous60940259
1170268200170268201CT32GENIChomozygous61908944
1170268248170268249GT42GENIChomozygous60940260
1170269050170269051AC31GENIChomozygous60940262
1170269357170269358AG28GENIChomozygous60940263
1170269412170269413AG23GENIChomozygous60940264
1170269505170269506GA15GENIChomozygous61908945
1170270337170270338GA5GENIChomozygous60940267
1170271167170271168TC28GENIChomozygous60940269
1170271631170271632GA45GENIChomozygous60940270
1170271934170271935AG16GENIChomozygous60940271
1170272091170272102AAAAAAAAAAA-----------28GENIChomozygous60940272
1170266219170266220CA26GENIChomozygous62271049
1170266220170266221AT25GENIChomozygous62271050
1170270084170270085AAGT8GENIChomozygous62271051