chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	226622471	226622472	A	G	41	GENIC	homozygous	108558817
1	226631657	226631658	G	A	37	GENIC	homozygous	108558818
1	226631979	226631980	T	C	30	GENIC	homozygous	108558819
1	226632065	226632066	T	C	29	GENIC	homozygous	108558820
1	226632145	226632146	G	A	41	GENIC	homozygous	108558821
1	226632174	226632175	T	G	40	GENIC	homozygous	108558822
1	226632517	226632518	C	T	45	GENIC	homozygous	108558823
1	226632974	226632975	G	A	39	GENIC	homozygous	108558824
1	226633105	226633106	C	T	44	GENIC	homozygous	108558825
1	226634743	226634744	C	A	34	GENIC	homozygous	108558827
1	226635194	226635195	G	A	24	GENIC	homozygous	108558828
1	226635792	226635793	A	G	46	GENIC	homozygous	108558829
1	226636470	226636471	G	A	32	GENIC	homozygous	108558830
1	226637997	226637998	A	C	49	GENIC	possibly homozygous	108558835
1	226638813	226638814	A	T	40	GENIC	homozygous	108558836
1	226638839	226638840	G	C	40	GENIC	possibly homozygous	108558837
1	226639578	226639579	T	C	41	GENIC	homozygous	108558839
1	226639699	226639700	G	T	59	GENIC	homozygous	108558840
1	226640970	226640971	T	C	49	GENIC	homozygous	108558842
1	226641283	226641284	A	G	39	GENIC	homozygous	108558843
1	226641956	226641957	T	C	41	GENIC	homozygous	108558844