chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	148419852	148419853	T	C	23	GENIC	homozygous	111769615
3	148420799	148420800	C	T	28	GENIC	homozygous	119714966
3	148421127	148421128	A	G	23	GENIC	homozygous	119744185
3	148422785	148422786	T	C	25	GENIC	homozygous	111769619
3	148423307	148423308	C	T	17	GENIC	homozygous	111769621
3	148424046	148424047	T	A	32	GENIC	homozygous	111769623
3	148424812	148424813	C	T	43	GENIC	homozygous	111769625
3	148425484	148425485	T	A	32	GENIC	homozygous	111769627
3	148425875	148425876	T	C	23	GENIC	homozygous	111769629
3	148425907	148425908	A	G	19	GENIC	homozygous	111769631
3	148426349	148426350	A	C	29	GENIC	homozygous	119744186
3	148426351	148426352	A	T	29	GENIC	homozygous	119744187
3	148426355	148426356	A	G	26	GENIC	homozygous	119744188
3	148426931	148426932	A	C	28	GENIC	homozygous	111769633
3	148427433	148427434	G	A	20	GENIC	homozygous	119744189
3	148427450	148427451	G	A	23	GENIC	homozygous	111769635
3	148427461	148427462	C	G	23	GENIC	homozygous	111769637
3	148427790	148427791	G	A	27	GENIC	homozygous	119744190
3	148427793	148427794	G	C	29	GENIC	homozygous	111769641