chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	37561487	37561488	A	T	33	GENIC	homozygous	115493857
12	37564004	37564005	C	A	28	GENIC	homozygous	115320933
12	37565009	37565010	G	A	30	GENIC	homozygous	115475783
12	37567045	37567046	T	C	23	GENIC	homozygous	115320939
12	37567276	37567277	A	C	28	GENIC	homozygous	115320941
12	37567397	37567398	T	C	25	GENIC	homozygous	115320943
12	37569431	37569432	G	A	23	GENIC	homozygous	115475787
12	37569481	37569482	C	G	25	GENIC	homozygous	115320949
12	37570023	37570024	T	A	28	GENIC	homozygous	115475789
12	37572573	37572574	G	A	22	GENIC	homozygous	115475791
12	37566834	37566835	A	G	13	GENIC	homozygous	115440064
12	37574852	37574853	C	G	2	GENIC	homozygous	115582971
12	37579482	37579483	T	C	21	GENIC	homozygous	115320971
12	37579916	37579917	G	T	34	GENIC	homozygous	115320973
12	37579917	37579918	A	G	32	GENIC	homozygous	115320975
12	37579958	37579959	C	T	39	GENIC	homozygous	115320977
12	37579962	37579963	G	A	35	GENIC	homozygous	115475797