chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	53386904	53386905	A	-	4	GENIC	homozygous	52632591
8	53386910	53386911	G	-	3	GENIC	homozygous	52632593
8	53386914	53386915	G	-	3	GENIC	homozygous	52632595
8	53386921	53386922	G	-	4	GENIC	homozygous	52632597
8	53386949	53386950	G	-	3	GENIC	homozygous	52632599
8	53386952	53386953	G	-	3	GENIC	homozygous	52632601
8	53386956	53386957	G	-	1	GENIC	homozygous	52632603
8	53387060	53387061	C	-	15	GENIC	homozygous	52632605
8	53387062	53387063	C	-	15	GENIC	homozygous	52632607
8	53387067	53387068	C	-	14	GENIC	homozygous	52632609
8	53387069	53387071	GT	--	15	GENIC	homozygous	52632611
8	53387074	53387075	G	-	15	GENIC	homozygous	52632613
8	53387079	53387080	G	-	21	GENIC	homozygous	52632615
8	53387086	53387087	C	-	22	GENIC	homozygous	52632617
8	53387091	53387092	C	-	22	GENIC	homozygous	52632619
8	53387096	53387097	C	-	23	GENIC	homozygous	52632621
8	53387103	53387104	C	-	23	GENIC	homozygous	52632623
8	53387108	53387109	C	-	24	GENIC	homozygous	52632625
8	53387114	53387115	G	-	21	GENIC	homozygous	52632627
8	53387121	53387122	C	-	18	GENIC	homozygous	52632629
8	53387137	53387138	T	-	33	GENIC	homozygous	52632631
8	53387534	53387535	C	T	51	GENIC	homozygous	52632633
8	53388098	53388099	C	CGTGTGT	33	GENIC	possibly homozygous	52632635
8	53388098	53388099	C	CGTGT	33	GENIC	heterozygous	52632637
8	53388117	53388118	C	G	63	GENIC	heterozygous	52632639
8	53389832	53389833	A	G	51	GENIC	homozygous	52632641
8	53390008	53390009	G	A	39	GENIC	homozygous	52632643
8	53390106	53390107	T	TCATCC	53	GENIC	homozygous	52632645
8	53390449	53390450	A	G	45	GENIC	homozygous	52632647
8	53390491	53390492	C	T	44	GENIC	homozygous	52632649
8	53390914	53390915	C	T	61	GENIC	homozygous	52632651
8	53391210	53391211	C	T	43	GENIC	homozygous	52632653
8	53391226	53391228	AA	--	42	GENIC	homozygous	52632655
8	53391320	53391321	C	T	31	GENIC	homozygous	52632657
8	53391570	53391571	C	T	32	GENIC	homozygous	52632659