chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	164829925	164829926	T	C	29	GENIC	homozygous	109340676
1	164830264	164830265	T	C	22	GENIC	homozygous	108953666
1	164830358	164830359	T	C	22	GENIC	possibly homozygous	108953668
1	164830430	164830431	T	C	23	GENIC	possibly homozygous	108953670
1	164830533	164830534	C	T	37	GENIC	possibly homozygous	109340678
1	164830623	164830624	C	T	22	GENIC	possibly homozygous	108953671
1	164831329	164831330	G	A	22	GENIC	homozygous	109340680
1	164831709	164831710	G	A	29	GENIC	homozygous	109340682
1	164832458	164832459	T	G	32	GENIC	homozygous	108953676
1	164834370	164834371	C	G	29	GENIC	possibly homozygous	108953679
1	164834972	164834973	T	C	34	GENIC	homozygous	108953680
1	164836012	164836013	T	A	25	GENIC	possibly homozygous	108953683
1	164840289	164840290	T	A	20	GENIC	possibly homozygous	109340684
1	164840389	164840390	A	T	23	GENIC	possibly homozygous	109340686
1	164841418	164841419	A	G	25	GENIC	homozygous	108953687
1	164841647	164841648	G	A	31	GENIC	homozygous	108953689
1	164844052	164844053	G	A	23	GENIC	homozygous	108953692
1	164844171	164844172	T	C	23	GENIC	possibly homozygous	108953694
1	164844172	164844173	G	A	24	GENIC	possibly homozygous	108953695
1	164844330	164844331	C	A	31	GENIC	possibly homozygous	109340688
1	164845068	164845069	G	A	36	GENIC	possibly homozygous	108953697
1	164845729	164845730	A	G	28	GENIC	possibly homozygous	108953698
1	164848047	164848048	G	A	23	GENIC	homozygous	108953708
1	164848085	164848086	G	A	21	GENIC	possibly homozygous	108953710
1	164848219	164848220	G	C	19	GENIC	heterozygous	109340692
1	164848955	164848956	C	T	25	GENIC	homozygous	109340694
1	164849360	164849361	G	A	24	GENIC	possibly homozygous	108953711