chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	10821644	10821645	C	T	16	GENIC	homozygous	45087467
X	10822571	10822572	C	T	21	GENIC	homozygous	45087468
X	10823302	10823303	G	A	11	GENIC	homozygous	45087469
X	10824239	10824241	CC	--	5	GENIC	homozygous	45087470
X	10824396	10824397	A	AT	19	GENIC	homozygous	45087471
X	10826469	10826470	A	G	17	GENIC	homozygous	45087472
X	10828955	10828956	T	C	19	GENIC	homozygous	45087473
X	10829332	10829333	G	A	19	GENIC	homozygous	45087474
X	10829546	10829547	T	-	10	GENIC	homozygous	45087475
X	10829807	10829808	T	C	17	GENIC	homozygous	45087476
X	10830003	10830004	A	G	19	GENIC	homozygous	45087477
X	10830307	10830308	G	A	18	GENIC	homozygous	45087478
X	10830402	10830403	A	G	11	GENIC	homozygous	45087479
X	10831960	10831961	G	C	9	GENIC	homozygous	45087480
X	10833152	10833153	G	A	18	GENIC	homozygous	45087483
X	10833361	10833362	A	C	16	GENIC	homozygous	45087484
X	10835187	10835188	T	C	14	GENIC	homozygous	45087485
X	10835446	10835447	A	G	10	GENIC	homozygous	45087486
X	10836431	10836432	G	GA	11	GENIC	possibly homozygous	45087490
X	10836481	10836482	T	C	18	GENIC	homozygous	45087491
X	10836968	10836971	TTG	---	9	GENIC	homozygous	45628723
X	10837463	10837464	T	C	13	GENIC	homozygous	45087494
X	10837490	10837491	A	-	12	GENIC	homozygous	45087495
X	10837503	10837504	A	G	14	GENIC	homozygous	45087496
X	10838826	10838827	C	T	13	GENIC	homozygous	45087497
X	10839756	10839757	G	C	20	GENIC	homozygous	45087498