chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	250785607	250785608	C	T	24	GENIC	homozygous	111292788
2	250786015	250786016	G	A	3	GENIC	homozygous	111292789
2	250786059	250786060	A	G	2	GENIC	homozygous	111292790
2	250786138	250786139	G	C	10	GENIC	homozygous	110850869
2	250786143	250786144	C	G	11	GENIC	homozygous	110850871
2	250791049	250791050	G	A	20	GENIC	homozygous	111292791
2	250791547	250791548	A	G	22	GENIC	homozygous	111292792
2	250794969	250794970	A	G	18	GENIC	homozygous	110379846
2	250795145	250795146	A	T	29	GENIC	heterozygous	111292793
2	250798466	250798467	T	A	15	GENIC	homozygous	110379856
2	250800614	250800615	C	A	14	GENIC	heterozygous	111292794
2	250800617	250800618	C	A	14	GENIC	possibly homozygous	111292795
2	250800618	250800619	G	A	14	GENIC	homozygous	111292796
2	250800721	250800722	A	T	28	GENIC	homozygous	110379860
2	250801279	250801280	A	G	9	GENIC	heterozygous	111292797
2	250803663	250803664	C	T	20	GENIC	homozygous	110379863
2	250804353	250804354	A	G	34	GENIC	homozygous	110379865
2	250804719	250804720	G	C	23	GENIC	homozygous	110379869
2	250803083	250803084	C	A	26	GENIC	homozygous	111292799
2	250802989	250802990	C	T	12	GENIC	homozygous	111292798