chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	62130993	62130994	C	T	26	GENIC	homozygous	56918013
4	62133254	62133255	A	G	22	GENIC	homozygous	56918015
4	62134494	62134495	A	T	32	GENIC	homozygous	56918016
4	62135544	62135545	A	G	35	GENIC	possibly homozygous	56918017
4	62136148	62136149	A	G	25	GENIC	possibly homozygous	56918018
4	62138346	62138347	A	-	23	GENIC	homozygous	56918019
4	62139593	62139594	T	TG	22	GENIC	possibly homozygous	56918020
4	62143078	62143079	C	T	26	GENIC	homozygous	56918021
4	62145711	62145712	A	C	27	GENIC	homozygous	56918022
4	62148922	62148923	C	CCTT	28	GENIC	homozygous	56918023
4	62149129	62149130	G	T	22	GENIC	homozygous	56918024
4	62157933	62157934	A	G	19	GENIC	homozygous	56918026
4	62157974	62157975	A	-	9	GENIC	homozygous	56918027
4	62157986	62157987	C	CA	4	GENIC	heterozygous	58538730
4	62157987	62157988	A	-	4	GENIC	heterozygous	58406862
4	62158143	62158149	ACACAC	------	11	GENIC	heterozygous	58657564
4	62158769	62158770	T	C	28	GENIC	possibly homozygous	56918028
4	62159860	62159861	G	GGAA	25	GENIC	homozygous	56918029
4	62162905	62162906	C	T	18	GENIC	homozygous	56918031
4	62163222	62163223	T	G	31	GENIC	possibly homozygous	56918032
4	62163256	62163257	A	-	22	GENIC	possibly homozygous	56918033
4	62163620	62163621	T	TC	30	GENIC	homozygous	56918034
4	62163907	62163908	G	A	33	GENIC	homozygous	56918035
4	62164280	62164281	C	T	28	GENIC	homozygous	56918036