chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	249540394	249540395	T	C	43	GENIC	homozygous	110374951
2	249540807	249540808	T	A	74	GENIC	homozygous	110374953
2	249541077	249541078	C	A	50	GENIC	homozygous	110374955
2	249542938	249542939	C	A	75	GENIC	possibly homozygous	110374959
2	249542971	249542972	A	C	76	GENIC	homozygous	110374961
2	249543149	249543150	C	T	66	GENIC	homozygous	110374963
2	249543193	249543194	C	A	58	GENIC	homozygous	110374965
2	249543292	249543293	C	A	61	GENIC	homozygous	110374967
2	249543489	249543490	A	G	62	GENIC	homozygous	110374969
2	249543601	249543602	T	C	51	GENIC	homozygous	110374971
2	249543760	249543761	G	A	50	GENIC	homozygous	110374973
2	249544521	249544522	G	A	78	GENIC	homozygous	110374975
2	249544768	249544769	C	T	62	GENIC	homozygous	110374977
2	249544805	249544806	G	A	56	GENIC	homozygous	110374979
2	249544918	249544919	C	T	40	GENIC	possibly homozygous	110374980
2	249545081	249545082	G	A	74	GENIC	homozygous	110374982
2	249545213	249545214	T	C	62	GENIC	homozygous	110374984
2	249545462	249545463	C	T	53	GENIC	homozygous	110374986
2	249546937	249546938	C	T	65	GENIC	homozygous	110374988
2	249547385	249547386	T	C	48	GENIC	homozygous	110374990
2	249547706	249547707	G	A	59	GENIC	homozygous	110374992
2	249549440	249549441	C	T	76	GENIC	possibly homozygous	110374994
2	249549634	249549635	A	G	30	GENIC	homozygous	110374996
2	249550507	249550508	A	G	79	GENIC	possibly homozygous	110374998
2	249550685	249550686	T	C	78	GENIC	homozygous	110375000
2	249551133	249551134	A	G	64	GENIC	possibly homozygous	110375002
2	249551482	249551483	G	A	58	GENIC	homozygous	110375004