chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	148419122	148419123	C	T	65	GENIC	possibly homozygous	111769612
3	148419347	148419348	G	T	33	GENIC	heterozygous	111769613
3	148419852	148419853	T	C	45	GENIC	homozygous	111769615
3	148420175	148420176	A	G	27	GENIC	homozygous	111769617
3	148422785	148422786	T	C	60	GENIC	homozygous	111769619
3	148423307	148423308	C	T	45	GENIC	possibly homozygous	111769621
3	148424046	148424047	T	A	56	GENIC	homozygous	111769623
3	148424812	148424813	C	T	34	GENIC	homozygous	111769625
3	148425484	148425485	T	A	57	GENIC	homozygous	111769627
3	148425875	148425876	T	C	54	GENIC	homozygous	111769629
3	148425907	148425908	A	G	43	GENIC	homozygous	111769631
3	148426931	148426932	A	C	41	GENIC	possibly homozygous	111769633
3	148427450	148427451	G	A	56	GENIC	homozygous	111769635
3	148427461	148427462	C	G	63	GENIC	homozygous	111769637
3	148427701	148427702	A	G	43	GENIC	homozygous	111769639
3	148427793	148427794	G	C	44	GENIC	homozygous	111769641
3	148427999	148428000	T	A	33	GENIC	possibly homozygous	111769643
3	148428035	148428036	A	G	41	GENIC	homozygous	111769645