chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	77283143	77283144	C		7	GENIC	homozygous	129757198
X	77288887	77288887		A	9	GENIC	homozygous	129757199
X	77291652	77291653	A	G	11	GENIC	homozygous	108275033
X	77291653	77291654	G	A	11	GENIC	homozygous	108275035
X	77291659	77291660	C		12	GENIC	homozygous	129757200
X	77291677	77291678	T		11	GENIC	homozygous	129757201
X	77291701	77291702	T		11	GENIC	possibly homozygous	129757202
X	77291738	77291738		A	11	GENIC	homozygous	129757203
X	77291747	77291748	T		12	GENIC	homozygous	129757204
X	77291762	77291763	T		14	GENIC	homozygous	129757205
X	77291801	77291801		G	13	GENIC	homozygous	129757208
X	77291782	77291782		A	13	GENIC	homozygous	129757206
X	77291783	77291783		C	13	GENIC	homozygous	129757207