chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 117937084 117937085 G C 18 GENIC possibly homozygous 563888005 8 117937113 117937114 G A 16 GENIC possibly homozygous 563888006 8 117937599 117937600 T C 16 GENIC homozygous 563888007 8 117938840 117938841 C A 3 GENIC heterozygous 565288079 8 117938845 117938846 G - 2 GENIC homozygous 708469393 8 117938987 117938989 TC -- 18 GENIC possibly homozygous 708469394 8 117948034 117948035 T C 14 GENIC homozygous 563888008 8 117948142 117948143 T C 28 GENIC possibly homozygous 563888009 8 117948689 117948690 A - 1 GENIC homozygous 708469395 8 117952317 117952318 G - 3 GENIC heterozygous 708469396 8 117952318 117952319 G T 3 GENIC heterozygous 563888010 8 117952320 117952321 T C 3 GENIC heterozygous 565288080 8 117954073 117954074 C T 17 GENIC homozygous 563888011 8 117956795 117956796 C G 2 GENIC homozygous 565288081 8 117960587 117960588 G A 16 GENIC homozygous 563888012 8 117960691 117960694 GGG --- 8 GENIC homozygous 708469398 8 117962115 117962116 A G 30 GENIC possibly homozygous 563888013 8 117963462 117963463 T - 7 GENIC heterozygous 708469399 8 117963771 117963772 A G 22 GENIC possibly homozygous 563888014 8 117968702 117968703 T G 4 GENIC homozygous 563888015 8 117969150 117969151 T C 12 GENIC homozygous 563888016 8 117969446 117969447 A G 10 GENIC possibly homozygous 563888017 8 117969914 117969915 T TG 16 GENIC possibly homozygous 708469400 8 117972274 117972275 T - 3 GENIC homozygous 708469401