chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	22303879	22303880	A	T	13	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	14	GENIC	homozygous	108238721
X	22313293	22313294	G	T	13	GENIC	homozygous	108238723
X	22313294	22313295	G	A	13	GENIC	homozygous	108238726
X	22313309	22313310	G	T	13	GENIC	homozygous	108238728
X	22313327	22313328	G	A	18	GENIC	homozygous	108238732
X	22315567	22315568	A	G	16	GENIC	homozygous	108238734
X	22317154	22317155	A	G	6	GENIC	homozygous	108238736
X	22317664	22317665	A	G	10	GENIC	homozygous	108682503
X	22320192	22320193	T	C	18	GENIC	homozygous	108238738
X	22320332	22320333	A	G	23	GENIC	homozygous	108238740
X	22320935	22320936	A	T	13	GENIC	homozygous	108238742
X	22333078	22333079	C	A	6	GENIC	homozygous	108238744
X	22335805	22335806	T	C	9	GENIC	homozygous	108238748
X	22336315	22336316	G	A	15	GENIC	homozygous	108372807
X	22336316	22336317	C	T	15	GENIC	homozygous	108372809
X	22342287	22342288	C	T	8	GENIC	homozygous	108372813
X	22342297	22342298	C	T	6	GENIC	homozygous	108372815
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
X	22318978	22318979	T	C	18	GENIC	possibly homozygous	108743948
X	22332996	22332997	T	C	8	GENIC	homozygous	108618677
X	22334404	22334405	T	C	19	GENIC	heterozygous	119909972
X	22337062	22337063	G	C	8	GENIC	homozygous	119909973