chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	23168002	23168003	G	A	10	GENIC	homozygous	108239705
X	23168804	23168805	T	C	8	GENIC	homozygous	108239707
X	23169384	23169385	T	G	8	GENIC	homozygous	108239709
X	23170856	23170857	T	C	8	GENIC	homozygous	108239715
X	23171787	23171788	C	T	6	GENIC	homozygous	108239717
X	23173281	23173282	T	A	8	GENIC	homozygous	119990129
X	23173287	23173288	C	A	8	GENIC	homozygous	108524011
X	23173306	23173307	A	G	7	GENIC	homozygous	108239719
X	23173313	23173314	C	T	8	GENIC	homozygous	108239721
X	23173323	23173324	A	C	6	GENIC	homozygous	108239723
X	23173327	23173328	G	C	6	GENIC	homozygous	108239725
X	23173334	23173335	A	C	7	GENIC	homozygous	108239727
X	23174013	23174014	C	T	11	GENIC	homozygous	108239729
X	23174323	23174324	G	A	14	GENIC	homozygous	108239731
X	23176079	23176080	C	A	8	GENIC	homozygous	108730950
X	23177326	23177327	A	G	7	GENIC	homozygous	108239733
X	23177976	23177977	C	G	14	GENIC	homozygous	108239735
X	23178418	23178419	A	G	7	GENIC	homozygous	108239737
X	23180632	23180633	T	C	5	GENIC	homozygous	108239739
X	23180875	23180876	G	T	12	GENIC	homozygous	108239741
X	23181019	23181020	G	A	4	GENIC	homozygous	108239747
X	23181428	23181429	T	C	8	GENIC	homozygous	108239753
X	23181499	23181500	C	T	10	GENIC	homozygous	108239755
X	23173280	23173281	C	A	7	GENIC	homozygous	119910358
X	23176101	23176102	A	C	8	GENIC	homozygous	119910360
X	23176146	23176147	A	G	6	GENIC	homozygous	119910361
X	23180185	23180186	G	A	4	GENIC	homozygous	108439834
X	23180208	23180209	A	G	6	GENIC	homozygous	108439837
X	23185470	23185471	A	G	5	GENIC	homozygous	108239761