chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15695462	15695463	G	GAA	22	GENIC	homozygous	45097276
X	15695479	15695480	A	-	24	GENIC	homozygous	45097277
X	15695659	15695660	C	T	61	GENIC	homozygous	45097278
X	15697473	15697474	G	A	73	GENIC	homozygous	45097279
X	15697497	15697498	G	A	69	GENIC	homozygous	45097280
X	15699571	15699572	C	T	51	GENIC	homozygous	45097281
X	15699582	15699583	C	G	52	GENIC	homozygous	45097282
X	15700996	15700997	T	C	47	GENIC	homozygous	45097283
X	15701633	15701634	C	T	67	GENIC	possibly homozygous	45097284
X	15701653	15701654	C	T	74	GENIC	homozygous	45097285
X	15701906	15701907	T	C	50	GENIC	homozygous	45097286
X	15702094	15702096	TT	--	43	GENIC	heterozygous	45252066
X	15702095	15702096	T	-	43	GENIC	heterozygous	45097287
X	15702107	15702109	TC	--	46	GENIC	heterozygous	45252067
X	15703931	15703932	T	C	38	GENIC	homozygous	45097288
X	15706007	15706008	G	A	72	GENIC	possibly homozygous	45097289
X	15708086	15708087	C	T	43	GENIC	homozygous	45097291
X	15708864	15708865	G	A	65	GENIC	homozygous	45097292