chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 135664804 135664805 C T 26 GENIC homozygous 985209650 5 135665105 135665106 G T 17 GENIC homozygous 985209651 5 135666369 135666370 C T 13 GENIC homozygous 985209652 5 135668452 135668453 T C 18 GENIC homozygous 985209653 5 135669118 135669119 T C 13 GENIC homozygous 985209654 5 135669568 135669569 A G 10 GENIC homozygous 985209655 5 135669593 135669594 G A 13 GENIC homozygous 985209656 5 135669628 135669629 T C 16 GENIC homozygous 985209657 5 135669823 135669824 T C 22 GENIC homozygous 985209658 5 135669857 135669858 A C 20 GENIC homozygous 985209659 5 135671312 135671313 G A 8 GENIC homozygous 985209660 5 135672173 135672174 T C 19 GENIC homozygous 985209661 5 135672864 135672865 T C 11 GENIC homozygous 985209662 5 135673053 135673054 G A 10 GENIC homozygous 985209663 5 135673187 135673188 A G 9 GENIC homozygous 985209664 5 135673910 135673911 A G 20 GENIC homozygous 985209665 5 135673963 135673964 C T 20 GENIC homozygous 985209666 5 135674186 135674187 G A 8 GENIC homozygous 985209667 5 135674254 135674255 A G 15 GENIC homozygous 985209668 5 135674298 135674299 C T 19 GENIC homozygous 985209669 5 135674436 135674437 T C 23 GENIC homozygous 985209670 5 135674786 135674787 T C 20 GENIC homozygous 985209671 5 135674974 135674975 T C 20 GENIC homozygous 985209672 5 135675084 135675085 C T 18 GENIC homozygous 985209673