chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	114087470	114087471	G	A	44	GENIC	homozygous	112009862
3	114087568	114087569	G	A	36	GENIC	homozygous	112009864
3	114087836	114087837	A	G	53	GENIC	homozygous	112009866
3	114088155	114088156	A	G	54	GENIC	homozygous	112009868
3	114088552	114088553	T	C	56	GENIC	homozygous	111678194
3	114088725	114088726	C	G	74	GENIC	possibly homozygous	112009870
3	114088756	114088757	C	G	76	GENIC	homozygous	112009872
3	114088853	114088854	C	T	48	GENIC	homozygous	112009874
3	114089179	114089180	C	A	62	GENIC	homozygous	112009876
3	114089282	114089283	G	A	90	GENIC	homozygous	112009878
3	114089285	114089286	C	T	90	GENIC	homozygous	112009880
3	114089627	114089628	C	T	39	GENIC	homozygous	112009882
3	114089628	114089629	A	G	39	GENIC	homozygous	112009884
3	114089659	114089660	A	G	56	GENIC	homozygous	112009886
3	114089757	114089758	A	G	51	GENIC	homozygous	112009888
3	114090101	114090102	C	T	47	GENIC	homozygous	112009890
3	114090238	114090239	A	G	61	GENIC	homozygous	111678196
3	114091251	114091252	C	T	55	GENIC	homozygous	112009892
3	114091617	114091618	T	G	59	GENIC	homozygous	112009893
3	114092354	114092355	C	A	69	GENIC	possibly homozygous	112009895
3	114092743	114092744	T	C	55	GENIC	homozygous	111678199