chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	135053167	135053168	T	C	8	GENIC	homozygous	45315624
X	135053275	135053276	T	C	14	GENIC	homozygous	45315625
X	135053442	135053443	G	-	10	GENIC	homozygous	45315626
X	135054388	135054389	C	CACCCCCCA	3	GENIC	heterozygous	45797861
X	135055523	135055526	TTT	---	9	GENIC	homozygous	45315627
X	135055673	135055674	A	C	11	GENIC	homozygous	45315628
X	135055817	135055818	C	T	19	GENIC	homozygous	45315629
X	135056047	135056048	A	T	13	GENIC	homozygous	45315630
X	135056998	135056999	C	T	21	GENIC	homozygous	45315631
X	135057718	135057719	G	A	18	GENIC	homozygous	45315632
X	135057919	135057920	T	C	15	GENIC	homozygous	45315633
X	135058265	135058280	TAATAATAATAATAA	---------------	10	GENIC	homozygous	45315634
X	135058314	135058315	C	T	13	GENIC	homozygous	45315636
X	135059145	135059146	A	G	16	GENIC	homozygous	45315637
X	135059168	135059169	C	T	22	GENIC	homozygous	45315638
X	135059192	135059193	T	C	21	GENIC	homozygous	45315639
X	135059832	135059833	G	GA	12	GENIC	homozygous	45315640
X	135061762	135061763	G	A	17	GENIC	homozygous	45315641
X	135061902	135061903	C	CGT	4	GENIC	homozygous	45315642
X	135061903	135061904	A	G	11	GENIC	homozygous	45315643
X	135062313	135062314	A	T	15	GENIC	homozygous	45315648
X	135062541	135062542	T	G	12	GENIC	homozygous	45315649
X	135062795	135062796	C	CGTGTGTGTGTGTGTGT	4	GENIC	homozygous	45797862
X	135062947	135062948	G	A	13	GENIC	homozygous	45315651
X	135063148	135063149	C	G	10	GENIC	homozygous	45315652
X	135064261	135064262	C	T	20	GENIC	homozygous	45315653
X	135065869	135065871	AG	--	6	GENIC	homozygous	45315655
X	135066274	135066275	G	A	8	GENIC	homozygous	45315656
X	135066471	135066472	A	G	9	GENIC	homozygous	45315657
X	135067273	135067274	A	G	18	GENIC	homozygous	45315658
X	135067540	135067541	C	-	15	GENIC	homozygous	45315659