chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	68189255	68189256	A	C	12	GENIC	homozygous	108272834
X	68204326	68204327	C	G	18	GENIC	homozygous	108272836
X	68204327	68204328	C	A	19	GENIC	homozygous	108272838
X	68204328	68204329	C	A	19	GENIC	homozygous	108272840
X	68204429	68204430	A	C	16	GENIC	homozygous	108272852
X	68279239	68279240	A	C	7	GENIC	homozygous	108272862
X	68377127	68377128	T	G	13	GENIC	heterozygous	108596334
X	68377130	68377131	A	G	10	GENIC	heterozygous	108387604
X	68390988	68390989	C	A	13	GENIC	homozygous	108272866
X	68390989	68390990	A	G	13	GENIC	homozygous	108272868
X	68391016	68391017	C	G	16	GENIC	homozygous	108272870
X	68391045	68391046	G	T	12	GENIC	homozygous	108447957
X	68391052	68391053	A	C	13	GENIC	homozygous	108387634
X	68391057	68391058	T	A	16	GENIC	homozygous	108387636
X	68391075	68391076	C	A	13	GENIC	homozygous	108387638
X	68391094	68391095	C	G	20	GENIC	homozygous	108387640
X	68460651	68460652	G	A	5	GENIC	homozygous	108596336
X	68547485	68547486	C	T	15	GENIC	homozygous	108272876
X	68547486	68547487	C	G	15	GENIC	homozygous	108272878
X	68499316	68499317	G	A	2	GENIC	homozygous	108608513