chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41256042	41256043	T	C	17	GENIC	homozygous	115384906
12	41256093	41256094	T	C	13	GENIC	homozygous	115384908
12	41256134	41256135	A	G	21	GENIC	possibly homozygous	115384910
12	41256162	41256163	G	A	16	GENIC	possibly homozygous	115384912
12	41256447	41256448	G	T	25	GENIC	homozygous	115384914
12	41258311	41258312	A	G	32	GENIC	possibly homozygous	115384916
12	41258500	41258501	T	C	39	GENIC	possibly homozygous	115384918
12	41258567	41258568	A	T	27	GENIC	homozygous	115384920
12	41259030	41259031	T	C	25	GENIC	homozygous	115477941
12	41259287	41259288	C	G	22	GENIC	homozygous	115384924
12	41259321	41259322	T	C	13	GENIC	homozygous	115384926
12	41259411	41259412	C	T	23	GENIC	homozygous	115384928
12	41259651	41259652	G	C	19	GENIC	homozygous	115384930
12	41259655	41259656	A	T	19	GENIC	homozygous	115384932
12	41259908	41259909	T	C	17	GENIC	homozygous	115441919
12	41260044	41260045	A	G	12	GENIC	homozygous	115329742
12	41260653	41260654	A	G	16	GENIC	possibly homozygous	115384934
12	41260753	41260754	G	T	14	GENIC	homozygous	115384936
12	41260769	41260770	G	A	11	GENIC	homozygous	115384938
12	41260780	41260781	A	C	9	GENIC	homozygous	115384940
12	41260935	41260936	T	C	15	GENIC	homozygous	115441920
12	41261017	41261018	C	T	20	GENIC	homozygous	115384942
12	41262598	41262599	C	T	17	GENIC	homozygous	115384944
12	41262681	41262682	G	A	24	GENIC	homozygous	115384946
12	41264102	41264103	C	T	33	GENIC	homozygous	115329750
12	41265046	41265047	C	T	15	GENIC	homozygous	115384948
12	41265081	41265082	C	T	20	GENIC	homozygous	115384950
12	41265639	41265640	C	T	17	GENIC	homozygous	115384952
12	41265750	41265751	C	T	17	GENIC	homozygous	115384954
12	41265751	41265752	C	T	17	GENIC	homozygous	115384956
12	41266337	41266338	G	C	29	GENIC	homozygous	115384958
12	41266394	41266395	C	G	19	GENIC	homozygous	115384960
12	41266409	41266410	C	A	17	GENIC	homozygous	115384962