chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	226621899	226621900	C	T	24	GENIC	heterozygous	108558815
1	226622471	226622472	A	G	71	GENIC	possibly homozygous	108558817
1	226628989	226628990	A	T	59	GENIC	possibly homozygous	108771889
1	226631657	226631658	G	A	70	GENIC	homozygous	108558818
1	226631979	226631980	T	C	46	GENIC	possibly homozygous	108558819
1	226632065	226632066	T	C	58	GENIC	possibly homozygous	108558820
1	226632145	226632146	G	A	54	GENIC	homozygous	108558821
1	226632174	226632175	T	G	69	GENIC	homozygous	108558822
1	226632517	226632518	C	T	53	GENIC	homozygous	108558823
1	226632614	226632615	T	G	37	GENIC	possibly homozygous	108771890
1	226632974	226632975	G	A	50	GENIC	homozygous	108558824
1	226633105	226633106	C	T	47	GENIC	homozygous	108558825
1	226633600	226633601	C	T	25	GENIC	possibly homozygous	108558826
1	226634743	226634744	C	A	50	GENIC	homozygous	108558827
1	226635194	226635195	G	A	39	GENIC	possibly homozygous	108558828
1	226635792	226635793	A	G	38	GENIC	homozygous	108558829
1	226636470	226636471	G	A	69	GENIC	homozygous	108558830
1	226636814	226636815	A	G	42	GENIC	possibly homozygous	108558831
1	226636828	226636829	G	T	42	GENIC	possibly homozygous	108558832
1	226636833	226636834	G	A	48	GENIC	heterozygous	108558833
1	226637026	226637027	C	T	28	GENIC	homozygous	108558834
1	226637731	226637732	T	C	13	GENIC	possibly homozygous	108771891
1	226637997	226637998	A	C	50	GENIC	homozygous	108558835
1	226638813	226638814	A	T	73	GENIC	possibly homozygous	108558836
1	226638839	226638840	G	C	80	GENIC	possibly homozygous	108558837
1	226639029	226639030	C	T	53	GENIC	possibly homozygous	108558838
1	226639578	226639579	T	C	71	GENIC	homozygous	108558839
1	226639699	226639700	G	T	56	GENIC	homozygous	108558840
1	226640215	226640216	C	A	45	GENIC	homozygous	108558841
1	226640970	226640971	T	C	55	GENIC	homozygous	108558842
1	226641283	226641284	A	G	48	GENIC	possibly homozygous	108558843
1	226641956	226641957	T	C	40	GENIC	possibly homozygous	108558844