chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	62130993	62130994	C	T	35	GENIC	homozygous	56918013
4	62131744	62131746	CA	--	27	GENIC	homozygous	56918014
4	62133254	62133255	A	G	34	GENIC	homozygous	56918015
4	62134494	62134495	A	T	33	GENIC	homozygous	56918016
4	62135544	62135545	A	G	49	GENIC	homozygous	56918017
4	62136148	62136149	A	G	39	GENIC	homozygous	56918018
4	62139593	62139594	T	TG	24	GENIC	homozygous	56918020
4	62143078	62143079	C	T	46	GENIC	homozygous	56918021
4	62145711	62145712	A	C	36	GENIC	homozygous	56918022
4	62148922	62148923	C	CCTT	29	GENIC	homozygous	56918023
4	62149129	62149130	G	T	29	GENIC	homozygous	56918024
4	62156455	62156456	A	-	8	GENIC	heterozygous	56918025
4	62157933	62157934	A	G	24	GENIC	possibly homozygous	56918026
4	62157974	62157975	A	-	12	GENIC	possibly homozygous	56918027
4	62158769	62158770	T	C	31	GENIC	possibly homozygous	56918028
4	62159860	62159861	G	GGAA	21	GENIC	homozygous	56918029
4	62162795	62162796	G	GCC	6	GENIC	homozygous	56918030
4	62162798	62162799	T	C	17	GENIC	homozygous	57330705
4	62162807	62162808	G	C	13	GENIC	heterozygous	57330707
4	62162905	62162906	C	T	24	GENIC	homozygous	56918031
4	62163222	62163223	T	G	25	GENIC	homozygous	56918032
4	62163256	62163257	A	-	1	GENIC	homozygous	56918033
4	62163620	62163621	T	TC	16	GENIC	homozygous	56918034
4	62163907	62163908	G	A	33	GENIC	homozygous	56918035
4	62164280	62164281	C	T	40	GENIC	homozygous	56918036