chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 99279675 99279675 A 45 GENIC homozygous 129089863 13 99279733 99279734 G 31 GENIC homozygous 129089864 13 99279896 99279897 C 36 GENIC homozygous 129089865 13 99279903 99279904 C 37 GENIC homozygous 129089866 13 99279911 99279912 T 34 GENIC homozygous 129089867 13 99279920 99279921 C 37 GENIC homozygous 129089868 13 99279933 99279934 C 36 GENIC homozygous 129089869 13 99279953 99279953 C 44 GENIC homozygous 129089870 13 99279960 99279961 G 46 GENIC homozygous 129089871 13 99288243 99288244 G A 41 GENIC homozygous 114583141 13 99288248 99288248 C 43 GENIC homozygous 129089872 13 99288251 99288252 G C 43 GENIC homozygous 114583143 13 99288262 99288263 T A 42 GENIC homozygous 114583145 13 99288263 99288264 A T 42 GENIC homozygous 114693570 13 99288328 99288329 T 46 GENIC homozygous 129089876 13 99288256 99288256 A 43 GENIC homozygous 129089873 13 99288282 99288283 T 44 GENIC homozygous 129089874 13 99288295 99288295 G 42 GENIC homozygous 129089875 13 99288342 99288342 AT 46 GENIC homozygous 129089877 13 99288343 99288344 T C 47 GENIC homozygous 114583147 13 99288350 99288350 G 47 GENIC homozygous 129089878 13 99288359 99288360 A 46 GENIC homozygous 129089879 13 99288368 99288368 AA 45 GENIC homozygous 129089880 13 99288401 99288402 C 45 GENIC homozygous 129089881 13 99288442 99288442 T 47 GENIC homozygous 129089882 13 99288471 99288472 A 47 GENIC homozygous 129089883 13 99288502 99288503 A 45 GENIC homozygous 129089884 13 99288517 99288517 A 48 GENIC homozygous 129089885 13 99288521 99288521 C 49 GENIC homozygous 129089886 13 99288550 99288551 T 51 GENIC homozygous 129089887 13 99288566 99288569 CTT 49 GENIC homozygous 129089888 13 99288583 99288583 GC 52 GENIC homozygous 129089889 13 99288587 99288588 T 51 GENIC homozygous 129089890 13 99288657 99288657 C 48 GENIC homozygous 129089891 13 99288528 99288529 T C 46 GENIC homozygous 114905434 13 99288563 99288564 T A 48 GENIC homozygous 114905436