chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 26437421 26437422 T C 12 GENIC homozygous 62928017 X 26440405 26440406 G A 6 GENIC homozygous 62928020 X 26440419 26440420 G A 8 GENIC homozygous 63033348 X 26440597 26440598 A G 7 GENIC homozygous 63033349 X 26440900 26440901 G T 2 GENIC heterozygous 62928021 X 26440903 26440904 A T 2 GENIC homozygous 62928022 X 26440915 26440916 C A 1 GENIC homozygous 63080066 X 26440925 26440926 C G 1 GENIC homozygous 63080067 X 26440926 26440927 T G 1 GENIC homozygous 63080068 X 26440935 26440936 A C 2 GENIC homozygous 63080069 X 26440986 26440987 A C 4 GENIC homozygous 63033351 X 26440987 26440988 A T 4 GENIC homozygous 63033352 X 26441051 26441052 C A 4 GENIC homozygous 63033354 X 26441567 26441568 C T 7 GENIC homozygous 63033355 X 26442933 26442934 A G 7 GENIC possibly homozygous 63033356 X 26442937 26442938 G A 7 GENIC possibly homozygous 62928025 X 26443086 26443087 C T 14 GENIC homozygous 62928026