chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15833505	15833506	G	A	44	GENIC	homozygous	45273987
X	15833897	15833898	A	ATT	20	GENIC	homozygous	45097652
X	15833982	15833983	A	T	41	GENIC	homozygous	45273988
X	15835272	15835273	G	GT	42	GENIC	homozygous	45273989
X	15835364	15835365	T	A	35	GENIC	possibly homozygous	45252115
X	15835953	15835954	A	ATTTGTTTG	7	GENIC	homozygous	45097655
X	15836449	15836450	G	GCA	14	GENIC	homozygous	45273990
X	15836617	15836618	C	T	31	GENIC	homozygous	45273991
X	15836829	15836830	A	G	44	GENIC	possibly homozygous	45273992
X	15837043	15837044	G	C	40	GENIC	homozygous	45273993
X	15837190	15837191	T	TGAAAAGAAA	3	GENIC	homozygous	45273994
X	15837195	15837196	G	GAGGA	5	GENIC	homozygous	45273995
X	15838201	15838210	ATGCTTATA	---------	3	GENIC	homozygous	45097658