chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 264095442 264095443 A G 27 GENIC possibly homozygous 797256060 1 264095886 264095887 A G 31 GENIC homozygous 797256061 1 264097432 264097433 T C 48 GENIC homozygous 797256062 1 264097633 264097634 A C 29 GENIC homozygous 797256063 1 264097682 264097683 G A 31 GENIC homozygous 797256064 1 264098597 264098598 C T 36 GENIC homozygous 797256065 1 264098630 264098631 A G 33 GENIC homozygous 797256066 1 264098735 264098736 C T 62 GENIC heterozygous 797256067 1 264099882 264099883 C T 31 GENIC homozygous 797256068 1 264099931 264099932 C T 24 GENIC homozygous 797256069 1 264100059 264100060 T A 35 GENIC homozygous 797256070 1 264100188 264100189 A G 30 GENIC homozygous 797256071 1 264100432 264100433 G A 40 GENIC homozygous 797256072 1 264100637 264100638 T C 27 GENIC homozygous 797256073 1 264101191 264101192 T C 21 GENIC homozygous 797256074 1 264101219 264101220 C T 16 GENIC heterozygous 797256075 1 264101725 264101726 T A 28 GENIC possibly homozygous 797256076 1 264101841 264101842 A G 20 GENIC homozygous 797256077 1 264102013 264102014 G A 28 GENIC homozygous 797256078 1 264102022 264102023 C T 27 GENIC homozygous 797256079 1 264102091 264102092 G A 38 GENIC homozygous 797256080 1 264102112 264102113 T C 41 GENIC homozygous 797256081 1 264102373 264102374 G A 27 GENIC homozygous 797256082 1 264102418 264102419 T C 29 GENIC homozygous 797256083 1 264102632 264102633 C T 32 GENIC homozygous 797256084 1 264103104 264103105 G A 38 GENIC homozygous 797256085 1 264103285 264103286 A G 19 GENIC homozygous 797256086 1 264103682 264103683 C T 31 GENIC homozygous 797256087 1 264104414 264104415 G A 39 GENIC homozygous 797256088