chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	48600300	48600301	G	A	56	GENIC	homozygous	115346726
12	48600411	48600412	T	C	87	GENIC	homozygous	115346728
12	48600841	48600842	T	C	61	GENIC	homozygous	115346730
12	48600976	48600977	T	G	43	GENIC	homozygous	115346734
12	48601330	48601331	T	C	69	GENIC	possibly homozygous	115346736
12	48601589	48601590	T	A	33	GENIC	homozygous	115452130
12	48601676	48601677	T	C	36	GENIC	homozygous	115452132
12	48601790	48601791	G	A	54	GENIC	homozygous	115346738
12	48601942	48601943	G	A	47	GENIC	homozygous	115346740
12	48602401	48602402	A	G	38	GENIC	homozygous	115346742
12	48602545	48602546	T	C	60	GENIC	homozygous	115346744
12	48602820	48602821	T	C	71	GENIC	homozygous	115346746
12	48605176	48605177	A	G	73	GENIC	homozygous	115346748
12	48605491	48605492	A	G	54	GENIC	homozygous	115346750
12	48605644	48605645	T	C	44	GENIC	homozygous	115346752