chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 81817040 81817041 A G 14 GENIC possibly homozygous 671509859 9 81817135 81817136 G A 20 GENIC possibly homozygous 671509860 9 81817524 81817525 T A 22 GENIC homozygous 671509861 9 81818987 81818988 G A 16 GENIC possibly homozygous 671509862 9 81819267 81819268 G C 2 GENIC homozygous 671509863 9 81819746 81819747 A C 2 GENIC homozygous 671509864 9 81820089 81820090 C CCCT 2 GENIC homozygous 769057920 9 81820320 81820321 G GC 19 GENIC possibly homozygous 769057921 9 81821638 81821639 T C 16 GENIC possibly homozygous 671509865 9 81821711 81821712 G - 9 GENIC homozygous 769057922 9 81822264 81822265 A G 25 GENIC possibly homozygous 671509866 9 81823733 81823734 C T 13 GENIC possibly homozygous 671509867 9 81824415 81824416 A C 13 GENIC heterozygous 671509868 9 81824862 81824863 A G 13 GENIC homozygous 671509869 9 81824967 81824968 T C 14 GENIC possibly homozygous 671509870 9 81825517 81825518 T TTCGC 5 GENIC homozygous 769057924 9 81826137 81826138 G C 2 GENIC homozygous 671509871 9 81826694 81826695 G T 28 GENIC homozygous 671509872 9 81827725 81827726 T A 15 GENIC possibly homozygous 671509873 9 81827819 81827820 A G 16 GENIC possibly homozygous 671509874 9 81828023 81828024 T A 12 GENIC homozygous 671509875 9 81828059 81828060 T A 5 GENIC heterozygous 671509876 9 81828979 81828980 G A 11 GENIC homozygous 671509877