chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 111885367 111885369 AA -- 10 GENIC heterozygous 45328920 X 111891965 111891966 C CA 9 GENIC heterozygous 45195286 X 111893839 111893840 G - 2 GENIC homozygous 45195291 X 111895577 111895578 T TA 7 GENIC heterozygous 45195296 X 111899846 111899847 T - 13 GENIC homozygous 45195304 X 111901060 111901061 T G 5 GENIC homozygous 45195309 X 111901908 111901909 G T 5 GENIC homozygous 45195311 X 111902563 111902565 CA -- 1 GENIC homozygous 45520864 X 111886838 111886840 AC -- 4 GENIC heterozygous 45520856 X 111899925 111899927 CA -- 5 GENIC heterozygous 45520860 X 111887887 111887888 A T 3 GENIC homozygous 45550635 X 111887891 111887892 T TGGTAGAGCG 3 GENIC homozygous 45550637 X 111887893 111887894 T TTG 3 GENIC homozygous 45573151 X 111887897 111887898 A AGCAAG 3 GENIC homozygous 45573153 X 111887900 111887901 G - 2 GENIC homozygous 45573155 X 111918855 111918856 A - 3 GENIC heterozygous 45520868 X 111944105 111944106 T - 3 INTERGENIC heterozygous 45550639 X 111909078 111909080 CC -- 1 GENIC homozygous 45634359