chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	22303879	22303880	A	T	12	GENIC	homozygous	108238713
X	22307559	22307560	A	T	11	GENIC	homozygous	108238715
X	22311029	22311030	T	C	5	GENIC	homozygous	108238717
X	22312809	22312810	G	A	11	GENIC	homozygous	108238719
X	22313290	22313291	G	T	15	GENIC	homozygous	108238721
X	22313293	22313294	G	T	14	GENIC	homozygous	108238723
X	22313294	22313295	G	A	14	GENIC	homozygous	108238726
X	22313309	22313310	G	T	17	GENIC	homozygous	108238728
X	22313318	22313319	G	C	17	GENIC	homozygous	108238730
X	22313327	22313328	G	A	19	GENIC	homozygous	108238732
X	22315567	22315568	A	G	14	GENIC	homozygous	108238734
X	22317154	22317155	A	G	6	GENIC	homozygous	108238736
X	22320192	22320193	T	C	18	GENIC	homozygous	108238738
X	22320332	22320333	A	G	22	GENIC	homozygous	108238740
X	22320935	22320936	A	T	12	GENIC	homozygous	108238742
X	22333078	22333079	C	A	6	GENIC	homozygous	108238744
X	22335805	22335806	T	C	6	GENIC	homozygous	108238748
X	22343749	22343750	T	G	17	GENIC	homozygous	108238750
X	22346663	22346664	T	C	15	GENIC	homozygous	108238752
X	22348938	22348939	A	C	7	GENIC	homozygous	108238754