chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 264095442 264095443 A G 20 GENIC possibly homozygous 965886230 1 264095886 264095887 A G 19 GENIC homozygous 965886231 1 264097432 264097433 T C 25 GENIC homozygous 965886232 1 264097633 264097634 A C 32 GENIC homozygous 965886233 1 264097682 264097683 G A 29 GENIC possibly homozygous 965886234 1 264099882 264099883 C T 22 GENIC homozygous 965886235 1 264099931 264099932 C T 27 GENIC homozygous 965886236 1 264100059 264100060 T A 23 GENIC possibly homozygous 965886237 1 264100188 264100189 A G 14 GENIC homozygous 965886238 1 264100432 264100433 G A 37 GENIC homozygous 965886239 1 264100637 264100638 T C 37 GENIC homozygous 965886240 1 264100851 264100852 A G 23 GENIC homozygous 965886241 1 264100853 264100854 A T 25 GENIC homozygous 965886242 1 264101191 264101192 T C 12 GENIC homozygous 965886243 1 264101725 264101726 T A 25 GENIC homozygous 965886244 1 264101841 264101842 A G 15 GENIC homozygous 965886245 1 264102013 264102014 G A 23 GENIC possibly homozygous 965886246 1 264102022 264102023 C T 23 GENIC possibly homozygous 965886247 1 264102091 264102092 G A 24 GENIC homozygous 965886248 1 264102112 264102113 T C 24 GENIC homozygous 965886249 1 264102373 264102374 G A 18 GENIC homozygous 965886250 1 264102418 264102419 T C 26 GENIC homozygous 965886251 1 264102632 264102633 C T 25 GENIC homozygous 965886252 1 264103104 264103105 G A 8 GENIC homozygous 965886253 1 264103285 264103286 A G 16 GENIC homozygous 965886254 1 264103682 264103683 C T 26 GENIC homozygous 965886255 1 264104414 264104415 G A 20 GENIC possibly homozygous 965886256