chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 135128478 135128479 G C 40 GENIC homozygous 140706797 X 135128670 135128671 G A 25 GENIC homozygous 140706798 X 135128790 135128791 C T 34 GENIC homozygous 140706799 X 135130842 135130842 T 32 GENIC homozygous 140598645 X 135130881 135130882 A G 26 GENIC homozygous 140706800 X 135131440 135131441 A G 26 GENIC homozygous 140706801 X 135132493 135132494 G A 27 GENIC homozygous 140706802 X 135133730 135133731 G A 33 GENIC homozygous 140706803 X 135134607 135134607 TGTA 22 GENIC possibly homozygous 140598646 X 135134892 135134893 G A 35 GENIC homozygous 140706804 X 135135788 135135789 T C 26 GENIC possibly homozygous 140706805 X 135135873 135135874 A G 30 GENIC homozygous 140706806 X 135137111 135137111 A 23 GENIC homozygous 140598647