chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	249540394	249540395	T	C	18	GENIC	homozygous	110374951
2	249540807	249540808	T	A	28	GENIC	homozygous	110374953
2	249541077	249541078	C	A	37	GENIC	homozygous	110374955
2	249541253	249541254	T	G	38	GENIC	homozygous	111389798
2	249542869	249542870	C	T	26	GENIC	homozygous	111389800
2	249542938	249542939	C	A	30	GENIC	homozygous	110374959
2	249543149	249543150	C	T	35	GENIC	homozygous	110374963
2	249543292	249543293	C	A	37	GENIC	homozygous	110374967
2	249543489	249543490	A	G	31	GENIC	possibly homozygous	110374969
2	249543601	249543602	T	C	20	GENIC	homozygous	110374971
2	249543760	249543761	G	A	26	GENIC	homozygous	110374973
2	249543799	249543800	C	T	23	GENIC	homozygous	111389802
2	249544518	249544519	C	A	22	GENIC	homozygous	111389804
2	249545213	249545214	T	C	30	GENIC	homozygous	110374984
2	249545317	249545318	G	A	27	GENIC	homozygous	111389806
2	249545330	249545331	T	C	29	GENIC	homozygous	111389808
2	249545462	249545463	C	T	29	GENIC	homozygous	110374986
2	249546937	249546938	C	T	34	GENIC	homozygous	110374988
2	249547385	249547386	T	C	33	GENIC	homozygous	110374990
2	249548315	249548316	C	T	21	GENIC	homozygous	111389810
2	249549697	249549698	C	A	27	GENIC	homozygous	111389813
2	249550861	249550862	G	A	15	GENIC	homozygous	111389815
2	249550889	249550890	T	A	13	GENIC	homozygous	111389817