chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	257567470	257567471	T	C	27	GENIC	homozygous	111043817
2	257568120	257568121	T	A	33	GENIC	homozygous	111043819
2	257570476	257570477	T	C	29	GENIC	homozygous	111043821
2	257575049	257575050	C	T	28	GENIC	homozygous	111043823
2	257575087	257575088	C	A	27	GENIC	homozygous	111043825
2	257577082	257577083	T	G	13	GENIC	homozygous	110412151
2	257577792	257577793	T	C	22	GENIC	homozygous	111043829
2	257578536	257578537	C	T	18	GENIC	homozygous	110412153
2	257578910	257578911	C	T	18	GENIC	homozygous	111043831
2	257582937	257582938	C	T	18	GENIC	homozygous	111043833
2	257583297	257583298	T	C	11	GENIC	homozygous	111043835
2	257583314	257583315	A	G	10	GENIC	homozygous	111043837
2	257585122	257585123	C	G	22	GENIC	homozygous	120132450
2	257585448	257585449	T	C	28	GENIC	homozygous	111043839
2	257595980	257595981	T	A	21	GENIC	possibly homozygous	111043843
2	257597490	257597491	C	T	22	GENIC	homozygous	111043849
2	257598936	257598937	C	T	22	GENIC	homozygous	111043851
2	257599637	257599638	G	A	17	GENIC	homozygous	111043853
2	257600658	257600659	A	G	14	GENIC	homozygous	111043855
2	257600686	257600687	T	A	10	GENIC	homozygous	110412165
2	257601600	257601601	T	G	19	GENIC	homozygous	111043857