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	32	GENIC	homozygous	110374953
2	249543193	249543194	C	A	35	GENIC	possibly homozygous	110374965
2	249542938	249542939	C	A	19	GENIC	homozygous	110374959
2	249542971	249542972	A	C	21	GENIC	homozygous	110374961
2	249543149	249543150	C	T	32	GENIC	homozygous	110374963
2	249543292	249543293	C	A	28	GENIC	homozygous	110374967
2	249543489	249543490	A	G	22	GENIC	homozygous	110374969
2	249543601	249543602	T	C	26	GENIC	possibly homozygous	110374971
2	249543760	249543761	G	A	27	GENIC	homozygous	110374973
2	249544521	249544522	G	A	33	GENIC	homozygous	110374975
2	249544768	249544769	C	T	28	GENIC	homozygous	110374977
2	249544805	249544806	G	A	18	GENIC	homozygous	110374979
2	249544918	249544919	C	T	21	GENIC	possibly homozygous	110374980
2	249545213	249545214	T	C	31	GENIC	homozygous	110374984
2	249545462	249545463	C	T	25	GENIC	homozygous	110374986
2	249546117	249546118	C	T	28	GENIC	heterozygous	110848613
2	249541542	249541543	G	A	24	GENIC	homozygous	110848606
2	249541758	249541759	C	T	29	GENIC	homozygous	110848608
2	249542546	249542547	A	G	24	GENIC	homozygous	110848609
2	249544212	249544213	C	G	38	GENIC	homozygous	110848611
2	249546343	249546344	T	A	32	GENIC	homozygous	110848614
2	249546390	249546391	C	T	24	GENIC	homozygous	110848616
2	249547001	249547002	G	A	29	GENIC	homozygous	110848618
2	249547385	249547386	T	C	20	GENIC	homozygous	110374990
2	249548745	249548746	C	T	21	GENIC	homozygous	110848619
2	249549634	249549635	A	G	19	GENIC	homozygous	110374996
2	249550015	249550016	G	A	21	GENIC	homozygous	110848621
2	249550507	249550508	A	G	33	GENIC	homozygous	110374998
2	249550657	249550658	G	T	39	GENIC	homozygous	110848622
2	249550685	249550686	T	C	39	GENIC	homozygous	110375000
2	249550738	249550739	G	A	30	GENIC	homozygous	110848624
2	249551224	249551225	G	A	21	GENIC	homozygous	110848625