chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 29808454 29808455 T C 52 GENIC homozygous 796686434 X 29808756 29808757 T C 33 GENIC homozygous 796686435 X 29810809 29810810 G A 30 GENIC homozygous 796686436 X 29810875 29810876 C G 24 GENIC possibly homozygous 796686437 X 29811839 29811840 T C 44 GENIC homozygous 796686438 X 29811945 29811946 G A 52 GENIC homozygous 796686439 X 29812573 29812574 G A 48 GENIC homozygous 796686440 X 29814185 29814186 G T 42 GENIC possibly homozygous 796686441 X 29815656 29815657 A G 39 GENIC possibly homozygous 796686442 X 29816718 29816719 T C 31 GENIC possibly homozygous 796686443 X 29817224 29817225 T A 60 GENIC homozygous 796686444 X 29819728 29819729 T C 33 GENIC possibly homozygous 796686445 X 29821808 29821809 C A 45 GENIC homozygous 796686446 X 29824162 29824163 T G 59 GENIC possibly homozygous 796686447 X 29824975 29824976 C A 40 GENIC heterozygous 796686448