chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	58408480	58408481	T	TC	24	GENIC	homozygous	49768644
13	58408862	58408863	G	GT	27	GENIC	homozygous	49768647
13	58408911	58408912	C	CT	27	GENIC	homozygous	49768648
13	58411451	58411452	T	-	8	GENIC	heterozygous	50580639
13	58421744	58421745	T	TGGAGGTAGAGGACAGTTGACTGACCAGTAACAAGATA	27	GENIC	homozygous	50519437
13	58424530	58424531	T	TC	35	GENIC	homozygous	49768712
13	58426713	58426714	G	GCCCA	24	GENIC	homozygous	49768722
13	58429193	58429195	CC	--	1	GENIC	homozygous	50519438
13	58429194	58429195	C	CGAAG	1	GENIC	homozygous	50519439
13	58434171	58434172	A	AT	23	GENIC	homozygous	49768767
13	58434203	58434204	G	-	19	GENIC	homozygous	49768768
13	58434208	58434209	T	TA	19	GENIC	homozygous	49768769
13	58434218	58434219	G	GT	16	GENIC	homozygous	49768770
13	58434222	58434223	A	AT	15	GENIC	homozygous	49768771
13	58434226	58434227	A	AT	16	GENIC	homozygous	49768772
13	58434235	58434236	T	TG	15	GENIC	homozygous	49768773
13	58434248	58434249	T	TA	15	GENIC	homozygous	49768774
13	58443713	58443714	T	TTG	4	GENIC	heterozygous	50519442
13	58451361	58451363	GT	--	12	GENIC	heterozygous	50519443
13	58452152	58452153	A	T	11	GENIC	homozygous	49768819
13	58453627	58453630	GAA	---	11	GENIC	heterozygous	50580640
13	58459684	58459686	CT	--	9	GENIC	heterozygous	50519444