chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	48600300	48600301	G	A	20	GENIC	homozygous	115346726
12	48600411	48600412	T	C	21	GENIC	homozygous	115346728
12	48600841	48600842	T	C	18	GENIC	homozygous	115346730
12	48600974	48600975	T	G	14	GENIC	homozygous	115346732
12	48600976	48600977	T	G	16	GENIC	homozygous	115346734
12	48601330	48601331	T	C	27	GENIC	homozygous	115346736
12	48601589	48601590	T	A	14	GENIC	homozygous	115452130
12	48601790	48601791	G	A	20	GENIC	homozygous	115346738
12	48601942	48601943	G	A	23	GENIC	homozygous	115346740
12	48602401	48602402	A	G	14	GENIC	homozygous	115346742
12	48602477	48602478	C	T	7	GENIC	homozygous	115511966
12	48602545	48602546	T	C	17	GENIC	homozygous	115346744
12	48602820	48602821	T	C	21	GENIC	homozygous	115346746
12	48605176	48605177	A	G	29	GENIC	homozygous	115346748
12	48605491	48605492	A	G	46	GENIC	homozygous	115346750
12	48605644	48605645	T	C	26	GENIC	homozygous	115346752