chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262264170262265CCA14GENIChomozygous60940238
1170262755170262756CT23GENIChomozygous60940239
1170262801170262802AC38GENIChomozygous60940240
1170263138170263139TA29GENIChomozygous60940241
1170263194170263195TC32GENIChomozygous61908940
1170263253170263254AG37GENIChomozygous60940242
1170263352170263353GA25GENIChomozygous60940244
1170264133170264134AG24GENIChomozygous60940245
1170264186170264187AG33GENIChomozygous60940246
1170264222170264223GGGTTT28GENIChomozygous60940247
1170264757170264758CT28GENIChomozygous60940248
1170265057170265058GA32GENIChomozygous60940250
1170266888170266889CT34GENICpossibly homozygous61908941
1170266926170266927GC38GENICpossibly homozygous60940251
1170267007170267008CT33GENICpossibly homozygous60940252
1170267037170267038GA28GENIChomozygous60940253
1170267149170267150TC28GENIChomozygous60940254
1170267323170267324TC26GENIChomozygous60940256
1170267579170267580GA34GENICpossibly homozygous60940257
1170267593170267594TC34GENIChomozygous60940258
1170267799170267800TC34GENIChomozygous61908942
1170267843170267844AT28GENICpossibly homozygous61908943
1170267958170267959TC31GENIChomozygous60940259
1170266219170266220CA26GENIChomozygous62271049
1170266220170266221AT26GENIChomozygous62271050
1170268200170268201CT38GENIChomozygous61908944
1170268248170268249GT28GENIChomozygous60940260
1170269050170269051AC30GENIChomozygous60940262
1170269357170269358AG23GENIChomozygous60940263
1170269412170269413AG16GENIChomozygous60940264
1170269505170269506GA26GENIChomozygous61908945
1170270084170270085AAGT8GENIChomozygous62271051
1170270337170270338GA13GENIChomozygous60940267
1170271167170271168TC31GENIChomozygous60940269
1170271631170271632GA32GENIChomozygous60940270
1170271934170271935AG29GENICpossibly homozygous60940271
1170272091170272102AAAAAAAAAAA-----------31GENIChomozygous60940272