chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	9909003	9909004	C	T	44	GENIC	homozygous	112492801
4	9909203	9909204	C	T	52	GENIC	homozygous	112492803
4	9909388	9909389	T	C	46	GENIC	homozygous	112492805
4	9910254	9910255	T	G	34	GENIC	homozygous	112492807
4	9910737	9910738	G	A	38	GENIC	homozygous	112492809
4	9911788	9911789	A	G	46	GENIC	homozygous	112492811
4	9912187	9912188	A	G	33	GENIC	homozygous	112492813
4	9912203	9912204	T	G	44	GENIC	possibly homozygous	112492815
4	9912392	9912393	A	G	47	GENIC	homozygous	112492817
4	9912644	9912645	T	G	51	GENIC	possibly homozygous	112492819
4	9913201	9913202	T	C	52	GENIC	homozygous	112492821
4	9915277	9915278	G	A	48	GENIC	homozygous	112492823
4	9917549	9917550	A	T	32	GENIC	homozygous	112492825
4	9917673	9917674	A	T	23	GENIC	homozygous	112492827
4	9917871	9917872	G	A	42	GENIC	homozygous	112492829
4	9917908	9917909	A	G	46	GENIC	homozygous	112492831
4	9918694	9918695	G	A	56	GENIC	homozygous	112492833
4	9921014	9921015	T	C	28	GENIC	possibly homozygous	112492835
4	9921117	9921118	C	A	28	GENIC	homozygous	112492837
4	9921431	9921432	G	A	20	GENIC	homozygous	112492839