chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 135664103 135664104 G T 24 GENIC homozygous 952459645 5 135664105 135664106 G T 23 GENIC homozygous 952459646 5 135664804 135664805 C T 16 GENIC homozygous 952459647 5 135665105 135665106 G T 25 GENIC homozygous 952459648 5 135666369 135666370 C T 23 GENIC homozygous 952459649 5 135668452 135668453 T C 30 GENIC possibly homozygous 952459650 5 135669118 135669119 T C 24 GENIC homozygous 952459651 5 135669568 135669569 A G 22 GENIC homozygous 952459652 5 135669593 135669594 G A 24 GENIC homozygous 952459653 5 135669628 135669629 T C 21 GENIC homozygous 952459654 5 135669823 135669824 T C 24 GENIC homozygous 952459655 5 135669857 135669858 A C 25 GENIC homozygous 952459656 5 135672173 135672174 T C 26 GENIC homozygous 952459657 5 135672864 135672865 T C 22 GENIC homozygous 952459658 5 135673053 135673054 G A 23 GENIC homozygous 952459659 5 135673187 135673188 A G 12 GENIC homozygous 952459660 5 135673910 135673911 A G 32 GENIC homozygous 952459661 5 135673963 135673964 C T 32 GENIC homozygous 952459662 5 135674186 135674187 G A 20 GENIC possibly homozygous 952459663 5 135674254 135674255 A G 36 GENIC homozygous 952459664 5 135674298 135674299 C T 27 GENIC homozygous 952459665 5 135674436 135674437 T C 27 GENIC homozygous 952459666 5 135674786 135674787 T C 29 GENIC homozygous 952459667 5 135674974 135674975 T C 27 GENIC homozygous 952459668 5 135675084 135675085 C T 20 GENIC homozygous 952459669