chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 115104789 115104790 C T 16 GENIC heterozygous 45726868 X 115107850 115107851 G A 24 GENIC heterozygous 45726870 X 115115630 115115631 A G 116 GENIC heterozygous 45726889 X 115116084 115116085 C A 235 GENIC heterozygous 46000362 X 115116104 115116105 A T 223 GENIC heterozygous 46000363 X 115116134 115116135 T C 210 GENIC heterozygous 46000364 X 115118823 115118824 T - 33 GENIC heterozygous 45198592 X 115121970 115121971 G - 35 GENIC heterozygous 46000365 X 115122663 115122664 A G 86 GENIC heterozygous 46000581 X 115144386 115144387 G C 242 GENIC heterozygous 45198669 X 115144388 115144389 A G 247 GENIC heterozygous 45198670 X 115144939 115144940 G T 30 GENIC heterozygous 45265054 X 115146749 115146751 AG -- 17 GENIC heterozygous 45726915 X 115149120 115149121 A C 8 GENIC heterozygous 45198675 X 115149177 115149178 T G 19 GENIC heterozygous 45198676 X 115149178 115149179 C G 19 GENIC heterozygous 45198677 X 115154660 115154661 G T 38 GENIC heterozygous 45726936 X 115154662 115154663 C T 38 GENIC heterozygous 45726937