chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262264170262265CCA15GENICpossibly homozygous60940238
1170262755170262756CT19GENICheterozygous60940239
1170262801170262802AC19GENIChomozygous60940240
1170263138170263139TA21GENIChomozygous60940241
1170263194170263195TC20GENICpossibly homozygous61908940
1170263253170263254AG21GENIChomozygous60940242
1170263352170263353GA25GENICpossibly homozygous60940244
1170264133170264134AG16GENIChomozygous60940245
1170264186170264187AG14GENIChomozygous60940246
1170264222170264223GGGTTT1GENIChomozygous60940247
1170264757170264758CT15GENIChomozygous60940248
1170265057170265058GA9GENIChomozygous60940250
1170266219170266220CA16GENIChomozygous62271049
1170266220170266221AT16GENIChomozygous62271050
1170266424170266425GA8GENIChomozygous62642022
1170266888170266889CT21GENIChomozygous61908941
1170266926170266927GC25GENICpossibly homozygous60940251
1170267007170267008CT21GENIChomozygous60940252
1170267037170267038GA17GENICpossibly homozygous60940253
1170267149170267150TC20GENICpossibly homozygous60940254
1170267323170267324TC20GENIChomozygous60940256
1170267579170267580GA14GENIChomozygous60940257
1170267593170267594TC22GENIChomozygous60940258
1170267799170267800TC26GENICpossibly homozygous61908942
1170267843170267844AT26GENICpossibly homozygous61908943
1170267958170267959TC14GENICpossibly homozygous60940259
1170268200170268201CT8GENIChomozygous61908944
1170268248170268249GT30GENIChomozygous60940260
1170269050170269051AC15GENICpossibly homozygous60940262
1170269357170269358AG13GENIChomozygous60940263
1170269412170269413AG13GENIChomozygous60940264
1170269505170269506GA17GENIChomozygous61908945
1170270337170270338GA15GENIChomozygous60940267
1170271167170271168TC18GENICpossibly homozygous60940269
1170271631170271632GA15GENIChomozygous60940270
1170271934170271935AG17GENICpossibly homozygous60940271
1170272091170272102AAAAAAAAAAA-----------4GENIChomozygous60940272