chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 129798708 129798709 C T 14 GENIC homozygous 893197017 7 129799658 129799659 G A 8 GENIC homozygous 893197018 7 129800613 129800614 C T 23 GENIC homozygous 893197019 7 129803953 129803954 C G 11 GENIC homozygous 893197020 7 129804694 129804695 T G 25 GENIC possibly homozygous 893197021 7 129804776 129804777 T C 16 GENIC homozygous 893197022 7 129804821 129804822 G A 8 GENIC homozygous 893197023 7 129805161 129805162 T C 15 GENIC homozygous 893197024 7 129805282 129805283 A G 6 GENIC homozygous 893197025 7 129805315 129805316 T C 5 GENIC homozygous 893197026 7 129805327 129805328 G T 4 GENIC homozygous 893197027 7 129805454 129805455 C A 6 GENIC homozygous 893197028 7 129805543 129805544 G A 9 GENIC heterozygous 893197029 7 129806000 129806001 C T 17 GENIC homozygous 893197030 7 129806589 129806590 C T 20 GENIC homozygous 893197031 7 129807333 129807334 G A 20 GENIC homozygous 893197032 7 129807551 129807552 T G 9 GENIC heterozygous 893197033 7 129807636 129807637 C A 14 GENIC homozygous 893197034 7 129808777 129808778 C T 18 GENIC homozygous 893197035 7 129808911 129808912 G T 23 GENIC homozygous 893197036 7 129808987 129808988 A G 18 GENIC homozygous 893197037 7 129810320 129810321 T C 17 GENIC homozygous 893197038 7 129810349 129810350 T C 11 GENIC homozygous 893197039 7 129810795 129810796 C T 17 GENIC homozygous 893197040 7 129810829 129810830 G A 12 GENIC homozygous 893197041 7 129811223 129811224 A G 16 GENIC homozygous 893197042