chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94486866	94486867	G	C	11	GENIC	homozygous	52053563
9	94487529	94487530	C	T	24	GENIC	homozygous	52280663
9	94488368	94488369	G	T	27	GENIC	homozygous	52280664
9	94488689	94488707	CACACACACACACACACA	------------------	17	GENIC	possibly homozygous	52915583
9	94489668	94489669	C	T	32	GENIC	homozygous	52280665
9	94490270	94490271	A	AG	21	GENIC	homozygous	52280666
9	94490375	94490376	T	C	23	GENIC	homozygous	52280667
9	94490669	94490670	C	A	13	GENIC	homozygous	52053575
9	94490672	94490674	AA	--	13	GENIC	possibly homozygous	52280668
9	94491050	94491051	A	G	22	GENIC	homozygous	52053579
9	94491101	94491107	ACACAC	------	18	GENIC	heterozygous	52915584
9	94491382	94491383	T	C	21	GENIC	homozygous	52053583
9	94492018	94492019	T	A	19	GENIC	homozygous	52280673
9	94492047	94492048	G	A	23	GENIC	homozygous	52280674
9	94492281	94492282	C	A	20	GENIC	homozygous	52053589
9	94492466	94492467	C	T	30	GENIC	homozygous	52280675
9	94492497	94492498	G	GCA	28	GENIC	homozygous	52053593
9	94492893	94492894	G	-	24	GENIC	homozygous	52280676
9	94493500	94493506	ACACAC	------	23	GENIC	possibly homozygous	52280678
9	94493522	94493523	A	G	32	GENIC	homozygous	52280680
9	94494024	94494025	G	C	27	GENIC	homozygous	52280681
9	94494774	94494775	C	G	25	GENIC	homozygous	52280683
9	94494796	94494797	A	G	17	GENIC	homozygous	52053600
9	94494956	94494957	C	CTG	5	GENIC	homozygous	52053602