chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	165973056	165973057	G	C	30	GENIC	homozygous	108355825
1	165974802	165974803	G	A	18	GENIC	homozygous	108355826
1	165976795	165976796	T	G	44	GENIC	homozygous	108355831
1	165978191	165978192	C	A	20	GENIC	homozygous	108355833
1	165978787	165978788	A	T	38	GENIC	possibly homozygous	108355834
1	165981927	165981928	A	T	23	GENIC	homozygous	108355839
1	165984094	165984095	C	T	34	GENIC	homozygous	108954609
1	165984199	165984200	A	G	33	GENIC	homozygous	108355846
1	165984385	165984386	A	G	28	GENIC	homozygous	108355847
1	165986130	165986131	T	C	38	GENIC	homozygous	108355852
1	165987105	165987106	G	A	46	GENIC	homozygous	120729704
1	165990503	165990504	C	T	21	GENIC	homozygous	108355871
1	165990777	165990778	G	A	32	GENIC	homozygous	120729706
1	165992939	165992940	G	A	39	GENIC	homozygous	120729708
1	165993655	165993656	G	A	33	GENIC	homozygous	108355875
1	165993661	165993662	A	G	33	GENIC	homozygous	108355876
1	165994048	165994049	A	G	27	GENIC	homozygous	108954617
1	165994198	165994199	C	T	35	GENIC	homozygous	108954618
1	165995067	165995068	C	T	28	GENIC	homozygous	120509143
1	165995487	165995488	C	T	30	GENIC	homozygous	108954620
1	166005455	166005456	T	C	20	GENIC	homozygous	108355886
1	166005705	166005706	G	A	35	GENIC	homozygous	109163018
1	166007678	166007679	A	G	26	GENIC	homozygous	108355889
1	166007774	166007775	G	T	39	GENIC	homozygous	109163020