chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 89330095 89330096 A C 13 GENIC homozygous 114571572 13 89330487 89330488 G A 18 GENIC homozygous 114831268 13 89330516 89330517 A G 22 GENIC homozygous 114831270 13 89330726 89330727 C T 24 GENIC homozygous 114831272 13 89330892 89330893 T 22 GENIC homozygous 131133709 13 89332864 89332865 T A 18 GENIC homozygous 114831274 13 89333632 89333633 G A 28 GENIC homozygous 114571574 13 89335591 89335592 T C 28 GENIC homozygous 114571576 13 89336450 89336451 A G 22 GENIC homozygous 114571580 13 89332488 89332489 A 20 GENIC homozygous 131505454 13 89334017 89334018 G A 15 GENIC homozygous 115078787 13 89334206 89334206 GCACAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTT 17 GENIC heterozygous 133845799 13 89337796 89337797 T C 31 GENIC homozygous 114571586 13 89338123 89338242 GAGACCAACTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC 9 GENIC heterozygous 131133711 13 89338361 89338362 C T 19 GENIC homozygous 114831276 13 89338458 89338459 C T 15 GENIC homozygous 114831278 13 89340405 89340406 A G 24 GENIC homozygous 114571596 13 89341602 89341612 CACGCGCGCA 24 GENIC homozygous 131133713 13 89343113 89343114 G A 21 GENIC homozygous 114571613 13 89343264 89343265 G A 26 GENIC homozygous 114571615 13 89343495 89343496 T C 32 GENIC homozygous 114571617 13 89343543 89343544 T G 21 GENIC homozygous 114571621 13 89343580 89343580 T 20 GENIC homozygous 131133714 13 89343764 89343765 A G 29 GENIC homozygous 114831280 13 89343882 89343883 A C 24 GENIC homozygous 114831282