chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	134857308	134857309	T	A	14	GENIC	homozygous	108344146
X	134860398	134860399	G	C	15	GENIC	homozygous	108509078
X	134860608	134860609	G	A	11	GENIC	homozygous	108509080
X	134860657	134860658	A	G	13	GENIC	homozygous	108509082
X	134861131	134861132	G	A	10	GENIC	homozygous	108509084
X	134861361	134861362	C	G	10	GENIC	homozygous	108509086
X	134861802	134861803	C	T	11	GENIC	homozygous	108509087
X	134861805	134861806	C	T	12	GENIC	homozygous	108509089
X	134862134	134862135	G	A	6	GENIC	homozygous	108509091
X	134862572	134862573	C	A	21	GENIC	homozygous	108509093
X	134863009	134863010	G	A	6	GENIC	homozygous	108509095
X	134863073	134863074	A	G	13	GENIC	homozygous	108344150
X	134863663	134863664	G	A	10	GENIC	homozygous	108509097
X	134863976	134863977	C	T	21	GENIC	homozygous	108509099
X	134865103	134865104	G	A	11	GENIC	homozygous	108509101