chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	212707	212708	A	C	32	GENIC	heterozygous	49997088
12	212714	212715	C	G	40	GENIC	heterozygous	51053601
12	212722	212723	G	A	51	GENIC	heterozygous	50273450
12	212743	212744	A	G	54	GENIC	heterozygous	50273453
12	212754	212755	A	G	59	GENIC	heterozygous	50392132
12	212762	212763	C	G	60	GENIC	heterozygous	49997089
12	212782	212783	T	C	61	GENIC	heterozygous	50273455
12	212859	212860	A	G	29	GENIC	heterozygous	49997091
12	212868	212869	G	A	26	GENIC	heterozygous	49997092
12	212882	212883	C	G	25	GENIC	heterozygous	51053602
12	212928	212929	G	A	23	GENIC	heterozygous	49997093
12	212944	212945	G	A	29	GENIC	heterozygous	49997094
12	212993	212994	C	T	49	GENIC	heterozygous	49997095
12	213012	213013	T	C	51	GENIC	heterozygous	49997096
12	213022	213023	C	A	53	GENIC	heterozygous	49997097
12	213030	213031	C	T	52	GENIC	heterozygous	51053603
12	213042	213043	T	C	54	GENIC	heterozygous	51053604
12	213062	213063	C	T	49	GENIC	heterozygous	49997098
12	213142	213143	T	C	9	GENIC	homozygous	49997099
12	213163	213164	A	G	4	GENIC	homozygous	49997100
12	213214	213215	G	A	18	GENIC	heterozygous	51053605