chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15695462	15695463	G	GAA	7	GENIC	homozygous	45097276
X	15695479	15695480	A	-	8	GENIC	homozygous	45097277
X	15696379	15696380	G	A	12	GENIC	homozygous	45273859
X	15697473	15697474	G	A	9	GENIC	homozygous	45097279
X	15697497	15697498	G	A	8	GENIC	homozygous	45097280
X	15699571	15699572	C	T	10	GENIC	homozygous	45097281
X	15699582	15699583	C	G	11	GENIC	homozygous	45097282
X	15699929	15699930	G	A	11	GENIC	homozygous	45273860
X	15701633	15701634	C	T	14	GENIC	homozygous	45097284
X	15701906	15701907	T	C	13	GENIC	homozygous	45097286
X	15702094	15702096	TT	--	8	GENIC	homozygous	45252066
X	15702107	15702109	TC	--	11	GENIC	heterozygous	45252067
X	15703313	15703314	G	GTTTTTTT	4	GENIC	homozygous	45273861
X	15703931	15703932	T	C	7	GENIC	homozygous	45097288
X	15704757	15704758	G	A	3	GENIC	heterozygous	45273862
X	15704762	15704763	A	T	3	GENIC	heterozygous	45273863
X	15704795	15704796	T	G	4	GENIC	homozygous	45273864
X	15706007	15706008	G	A	17	GENIC	homozygous	45097289
X	15708086	15708087	C	T	8	GENIC	homozygous	45097291
X	15708864	15708865	G	A	16	GENIC	homozygous	45097292