chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	45077094	45077095	A	-	12	GENIC	heterozygous	52614503
8	45087395	45087396	A	-	19	GENIC	heterozygous	52614544
8	45088930	45088931	G	GGTGTGTGT	19	GENIC	heterozygous	52614550
8	45088931	45088933	GT	--	19	GENIC	heterozygous	53105701
8	45092839	45092841	TT	--	15	GENIC	heterozygous	52614580
8	45092840	45092841	T	-	15	GENIC	heterozygous	53105704
8	45103804	45103805	C	CCAT	23	GENIC	heterozygous	52614640
8	45111493	45111494	C	G	27	GENIC	homozygous	52614679
8	45112770	45112771	G	-	19	GENIC	homozygous	52614696
8	45112817	45112818	G	-	17	GENIC	homozygous	52614698
8	45121350	45121352	GT	--	19	GENIC	heterozygous	52614740
8	45127041	45127042	A	AG	14	GENIC	homozygous	52614762
8	45127044	45127045	A	-	13	GENIC	homozygous	52614764
8	45134889	45134890	G	-	37	GENIC	homozygous	52614805
8	45140201	45140203	AC	--	18	GENIC	possibly homozygous	52614844
8	45143864	45143865	A	-	19	GENIC	heterozygous	53181464