chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	37475482	37475483	G	T	11	GENIC	homozygous	108256567
X	37475515	37475516	A	T	11	GENIC	homozygous	108256569
X	37475681	37475682	G	A	15	GENIC	homozygous	108256571
X	37475907	37475908	C	A	21	GENIC	homozygous	108380360
X	37475933	37475934	G	T	22	GENIC	homozygous	108380362
X	37475934	37475935	T	G	21	GENIC	homozygous	108380364
X	37476036	37476037	C	A	20	GENIC	homozygous	108256573
X	37489689	37489690	T	C	21	GENIC	homozygous	108256575
X	37495239	37495240	G	T	15	GENIC	homozygous	108256577
X	37507201	37507202	C	T	13	GENIC	homozygous	108380366
X	37507402	37507403	C	T	16	GENIC	homozygous	108256579
X	37507484	37507485	G	T	29	GENIC	homozygous	108256581
X	37507572	37507573	A	G	18	GENIC	homozygous	108256583
X	37507706	37507707	C	T	18	GENIC	homozygous	108256585