chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 29808454 29808455 T C 14 GENIC homozygous 995691399 X 29808756 29808757 T C 16 GENIC homozygous 995691400 X 29810809 29810810 G A 12 GENIC homozygous 995691401 X 29810875 29810876 C G 11 GENIC homozygous 995691402 X 29811839 29811840 T C 11 GENIC homozygous 995691403 X 29811945 29811946 G A 17 GENIC possibly homozygous 995691404 X 29812573 29812574 G A 20 GENIC homozygous 995691405 X 29812848 29812849 A T 15 GENIC possibly homozygous 995691406 X 29813567 29813568 C T 8 GENIC homozygous 995691407 X 29814185 29814186 G T 13 GENIC homozygous 995691408 X 29814314 29814315 C T 15 GENIC possibly homozygous 995691409 X 29816718 29816719 T C 17 GENIC possibly homozygous 995691410 X 29817224 29817225 T A 13 GENIC possibly homozygous 995691411 X 29819728 29819729 T C 14 GENIC homozygous 995691412 X 29821808 29821809 C A 8 GENIC homozygous 995691413 X 29824696 29824697 A G 7 GENIC homozygous 995691414