chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	164830264	164830265	T	C	17	GENIC	homozygous	108953666
1	164830358	164830359	T	C	19	GENIC	homozygous	108953668
1	164830430	164830431	T	C	25	GENIC	homozygous	108953670
1	164830623	164830624	C	T	27	GENIC	homozygous	108953671
1	164830828	164830829	G	C	23	GENIC	homozygous	108953673
1	164831463	164831464	A	C	28	GENIC	homozygous	108953674
1	164832458	164832459	T	G	33	GENIC	homozygous	108953676
1	164833689	164833690	T	C	14	GENIC	homozygous	108953677
1	164834370	164834371	C	G	22	GENIC	homozygous	108953679
1	164834972	164834973	T	C	24	GENIC	homozygous	108953680
1	164835373	164835374	G	A	26	GENIC	homozygous	108953682
1	164836012	164836013	T	A	23	GENIC	homozygous	108953683
1	164839682	164839683	T	C	27	GENIC	homozygous	108953684
1	164840120	164840121	C	T	21	GENIC	homozygous	108953686
1	164841418	164841419	A	G	19	GENIC	homozygous	108953687
1	164841647	164841648	G	A	26	GENIC	homozygous	108953689
1	164842957	164842958	A	C	35	GENIC	homozygous	108953691
1	164844052	164844053	G	A	10	GENIC	homozygous	108953692
1	164844171	164844172	T	C	13	GENIC	homozygous	108953694
1	164844172	164844173	G	A	13	GENIC	homozygous	108953695
1	164845068	164845069	G	A	35	GENIC	homozygous	108953697
1	164845729	164845730	A	G	35	GENIC	homozygous	108953698
1	164846923	164846924	T	C	17	GENIC	homozygous	108953700
1	164846971	164846972	G	C	12	GENIC	homozygous	108953702
1	164847401	164847402	G	C	10	GENIC	homozygous	108953703
1	164847498	164847499	A	G	18	GENIC	homozygous	108953705
1	164847565	164847566	A	G	19	GENIC	homozygous	108953706
1	164848047	164848048	G	A	25	GENIC	homozygous	108953708
1	164848085	164848086	G	A	29	GENIC	homozygous	108953710
1	164849360	164849361	G	A	20	GENIC	homozygous	108953711
1	164849664	164849665	C	T	6	GENIC	homozygous	108953713