chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	164876258	164876259	T	C	13	GENIC	homozygous	108953784
1	164876616	164876617	G	A	16	GENIC	homozygous	108953785
1	164876883	164876884	G	A	28	GENIC	homozygous	108953787
1	164876981	164876982	T	C	18	GENIC	possibly homozygous	108953789
1	164878495	164878496	T	C	29	GENIC	homozygous	108953792
1	164879303	164879304	G	A	26	GENIC	homozygous	108953795
1	164879948	164879949	T	C	39	GENIC	homozygous	108953798
1	164881302	164881303	C	G	37	GENIC	homozygous	108953800
1	164881825	164881826	T	C	31	GENIC	homozygous	108953802
1	164882292	164882293	G	A	23	GENIC	homozygous	109340720
1	164882831	164882832	A	C	31	GENIC	homozygous	108953805
1	164884504	164884505	A	G	37	GENIC	homozygous	108953810
1	164884529	164884530	C	G	37	GENIC	homozygous	108953811
1	164884626	164884627	G	A	45	GENIC	homozygous	108953813
1	164884903	164884904	T	C	38	GENIC	homozygous	108953815
1	164885498	164885499	G	A	27	GENIC	homozygous	109435719
1	164885567	164885568	T	G	34	GENIC	homozygous	108953818
1	164885675	164885676	A	G	44	GENIC	homozygous	108953819
1	164886500	164886501	C	T	23	GENIC	homozygous	108953823
1	164889477	164889478	T	A	26	GENIC	homozygous	108953826
1	164891278	164891279	T	C	49	GENIC	homozygous	108953829
1	164894770	164894771	T	C	21	GENIC	homozygous	108953832
1	164896554	164896555	T	C	32	GENIC	homozygous	108953836
1	164896894	164896895	T	C	29	GENIC	possibly homozygous	108953837
1	164897493	164897494	T	G	20	GENIC	possibly homozygous	109340726
1	164897916	164897917	G	A	18	GENIC	heterozygous	108953839
1	164899999	164900000	C	A	39	GENIC	homozygous	109340730
1	164900384	164900385	G	C	17	GENIC	homozygous	108953845