chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	32332643	32332644	C	G	15	GENIC	homozygous	108478852
X	32337889	32337890	C	T	15	GENIC	homozygous	108252461
X	32338477	32338478	C	T	12	GENIC	homozygous	120025080
X	32341079	32341080	C	T	14	GENIC	homozygous	108478854
X	32343202	32343203	G	A	18	GENIC	homozygous	108478856
X	32346549	32346550	T	C	10	GENIC	homozygous	108478858
X	32350620	32350621	C	T	18	GENIC	homozygous	108478860
X	32357133	32357134	T	C	20	GENIC	homozygous	108478866
X	32357586	32357587	C	T	14	GENIC	homozygous	108478868
X	32358492	32358493	C	T	10	GENIC	homozygous	108478870
X	32358814	32358815	C	A	16	GENIC	homozygous	108478872
X	32360173	32360174	A	C	16	GENIC	homozygous	108478874
X	32360339	32360340	G	A	15	GENIC	heterozygous	120025081
X	32361601	32361602	C	A	11	GENIC	homozygous	108478876
X	32361846	32361847	A	G	13	GENIC	homozygous	108478878
X	32363831	32363832	C	G	12	GENIC	homozygous	108478880
X	32364917	32364918	G	A	14	GENIC	homozygous	108478882
X	32365007	32365008	C	T	12	GENIC	homozygous	108478884
X	32365620	32365621	A	G	15	GENIC	homozygous	108478886
X	32366450	32366451	A	G	17	GENIC	homozygous	108478888
X	32366694	32366695	C	A	11	GENIC	homozygous	108478890
X	32367468	32367469	C	T	13	GENIC	heterozygous	108817401
X	32367472	32367473	C	T	13	GENIC	heterozygous	108817402
X	32367596	32367597	A	T	12	GENIC	homozygous	108478892
X	32368734	32368735	A	G	15	GENIC	homozygous	108478894
X	32368911	32368912	A	G	15	GENIC	homozygous	108478896
X	32372257	32372258	A	G	8	GENIC	homozygous	108478900
X	32375886	32375887	G	A	9	GENIC	homozygous	108478902
X	32376301	32376302	T	C	9	GENIC	homozygous	108478904