chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	2126707	2126708	A	G	18	GENIC	homozygous	45076473
X	2128045	2128046	T	TC	10	GENIC	possibly homozygous	45076474
X	2128793	2128794	C	T	22	GENIC	homozygous	45076475
X	2131235	2131239	AAAC	----	10	GENIC	homozygous	45076476
X	2131412	2131413	G	GT	11	GENIC	homozygous	45076477