chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	2500795	2500796	C	A	16	GENIC	homozygous	45076793
X	2502569	2502570	G	-	11	GENIC	homozygous	45076794
X	2502570	2502571	G	A	11	GENIC	homozygous	45496853
X	2505227	2505228	G	A	9	GENIC	homozygous	45076795
X	2508777	2508778	C	T	13	GENIC	homozygous	45076796
X	2510482	2510483	T	-	9	GENIC	possibly homozygous	45076798
X	2510798	2510799	A	-	15	GENIC	homozygous	45076799