chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 59829761 59829762 T C 22 GENIC homozygous 116608848 10 59830008 59830009 C T 31 GENIC homozygous 116608850 10 59830162 59830163 G A 27 GENIC homozygous 116608852 10 59830384 59830385 C T 25 GENIC homozygous 116608854 10 59830934 59830935 T C 31 GENIC homozygous 116608856 10 59831668 59831669 G C 18 GENIC homozygous 116608858 10 59831748 59831749 G A 29 GENIC homozygous 116608860 10 59831819 59831820 C A 29 GENIC homozygous 116608862 10 59831972 59831973 C T 30 GENIC homozygous 116608864 10 59832312 59832313 T C 25 GENIC homozygous 116608866 10 59832674 59832675 G A 23 GENIC homozygous 116608868 10 59832857 59832858 G T 24 GENIC possibly homozygous 116608870 10 59832926 59832927 T C 17 GENIC homozygous 116608872 10 59833087 59833088 C T 25 GENIC homozygous 116608874 10 59834399 59834400 G T 23 GENIC homozygous 116608876 10 59834851 59834852 A T 19 GENIC homozygous 116608878 10 59834994 59834999 AAACC 14 GENIC homozygous 128820937 10 59837293 59837294 G A 25 GENIC homozygous 116608880 10 59837916 59837917 A G 24 GENIC homozygous 116608882 10 59838127 59838128 T A 24 GENIC homozygous 117060976 10 59838128 59838129 T A 24 GENIC homozygous 117060978 10 59839909 59839910 T C 19 GENIC homozygous 116608884 10 59840393 59840394 A G 22 GENIC homozygous 116608886 10 59840509 59840510 T G 18 GENIC homozygous 116608888 10 59840893 59840894 C T 21 GENIC homozygous 116608890 10 59842670 59842671 T C 25 GENIC homozygous 116608892 10 59842923 59842924 A G 22 GENIC homozygous 116608896 10 59843439 59843439 A 15 GENIC homozygous 128820938 10 59843956 59843957 T C 29 GENIC homozygous 116608898 10 59845448 59845449 A 30 GENIC homozygous 128820940 10 59845669 59845670 T C 15 GENIC homozygous 116608900 10 59847876 59847877 C T 28 GENIC possibly homozygous 116608902 10 59848444 59848445 C T 30 GENIC homozygous 116608904 10 59854673 59854674 T C 17 GENIC homozygous 116608908 10 59860050 59860051 G T 22 GENIC homozygous 116608910 10 59860894 59860895 G 24 GENIC homozygous 128820943