chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	37330395	37330396	T	C	7	INTERGENIC	homozygous	45754613
X	37330684	37330685	T	G	8	INTERGENIC	homozygous	45754616
X	37331468	37331469	C	T	14	INTERGENIC	homozygous	45937013
X	37333724	37333725	T	G	12	INTERGENIC	homozygous	45754622
X	37334394	37334395	T	G	12	INTERGENIC	homozygous	45754625
X	37335458	37335459	C	A	7	INTERGENIC	homozygous	45754627
X	37335978	37335979	T	C	8	INTERGENIC	homozygous	45754633
X	37336107	37336108	G	A	7	INTERGENIC	homozygous	45754635
X	37336165	37336166	G	C	10	INTERGENIC	homozygous	45754637
X	37338703	37338704	A	ACC	8	INTERGENIC	homozygous	45772169
X	37340579	37340580	T	C	7	INTERGENIC	homozygous	45754651
X	37340650	37340651	G	A	8	INTERGENIC	homozygous	45754653
X	37340968	37340969	A	AT	9	INTERGENIC	homozygous	45754655
X	37341117	37341118	G	T	13	INTERGENIC	homozygous	45754657
X	37341125	37341126	A	T	12	INTERGENIC	homozygous	45754659
X	37341143	37341144	A	AT	11	INTERGENIC	homozygous	45754661
X	37341613	37341614	C	T	9	INTERGENIC	homozygous	45754665
X	37341759	37341760	T	C	8	INTERGENIC	homozygous	45754668
X	37342150	37342151	T	C	10	INTERGENIC	homozygous	45754672
X	37342366	37342368	GT	--	10	INTERGENIC	homozygous	45754674
X	37343247	37343248	T	G	7	INTERGENIC	homozygous	45754676