chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15833505	15833506	G	A	10	GENIC	homozygous	45273987
X	15833674	15833675	T	-	14	GENIC	heterozygous	45097651
X	15833897	15833898	A	ATT	12	GENIC	possibly homozygous	45097652
X	15833897	15833898	A	AT	12	GENIC	heterozygous	45473857
X	15833982	15833983	A	T	12	GENIC	homozygous	45273988
X	15835272	15835273	G	GT	13	GENIC	homozygous	45273989
X	15835953	15835954	A	ATTTGTTTG	12	GENIC	homozygous	45097655
X	15836449	15836450	G	GCA	8	GENIC	heterozygous	45273990
X	15836617	15836618	C	T	17	GENIC	homozygous	45273991
X	15836829	15836830	A	G	11	GENIC	homozygous	45273992
X	15837043	15837044	G	C	13	GENIC	homozygous	45273993
X	15837186	15837187	A	AAAGGAGG	6	GENIC	homozygous	45473861
X	15837189	15837190	C	A	6	GENIC	homozygous	45473863
X	15837190	15837191	T	TGAAAAGAAA	6	GENIC	homozygous	45273994
X	15837192	15837193	C	A	6	GENIC	homozygous	45795328
X	15837195	15837196	G	GAGGA	6	GENIC	homozygous	45273995
X	15838201	15838210	ATGCTTATA	---------	3	GENIC	homozygous	45097658
X	15838325	15838329	CCCT	----	1	GENIC	homozygous	45795329