chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	249540394	249540395	T	C	21	GENIC	homozygous	110374951
2	249540807	249540808	T	A	37	GENIC	homozygous	110374953
2	249541077	249541078	C	A	22	GENIC	homozygous	110374955
2	249542938	249542939	C	A	27	GENIC	homozygous	110374959
2	249542971	249542972	A	C	34	GENIC	homozygous	110374961
2	249543149	249543150	C	T	31	GENIC	homozygous	110374963
2	249543193	249543194	C	A	21	GENIC	homozygous	110374965
2	249543292	249543293	C	A	29	GENIC	homozygous	110374967
2	249543489	249543490	A	G	30	GENIC	homozygous	110374969
2	249543601	249543602	T	C	16	GENIC	homozygous	110374971
2	249543760	249543761	G	A	35	GENIC	homozygous	110374973
2	249544521	249544522	G	A	26	GENIC	homozygous	110374975
2	249544768	249544769	C	T	20	GENIC	homozygous	110374977
2	249544805	249544806	G	A	14	GENIC	homozygous	110374979
2	249545081	249545082	G	A	24	GENIC	homozygous	110374982
2	249545213	249545214	T	C	18	GENIC	homozygous	110374984
2	249545462	249545463	C	T	22	GENIC	homozygous	110374986
2	249546937	249546938	C	T	20	GENIC	homozygous	110374988
2	249547385	249547386	T	C	27	GENIC	homozygous	110374990
2	249547706	249547707	G	A	28	GENIC	homozygous	110374992
2	249549440	249549441	C	T	43	GENIC	homozygous	110374994
2	249549634	249549635	A	G	19	GENIC	homozygous	110374996
2	249550507	249550508	A	G	36	GENIC	homozygous	110374998
2	249550685	249550686	T	C	14	GENIC	homozygous	110375000
2	249551133	249551134	A	G	13	GENIC	homozygous	110375002
2	249551482	249551483	G	A	23	GENIC	homozygous	110375004
2	249545882	249545883	C	T	26	GENIC	homozygous	120255044