chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	165483149	165483150	A	T	14	GENIC	homozygous	108353925
1	165483225	165483226	C	A	11	GENIC	homozygous	108353927
1	165483620	165483621	C	T	10	GENIC	homozygous	108353929
1	165483651	165483652	C	T	13	GENIC	homozygous	108353931
1	165483687	165483688	G	T	19	GENIC	homozygous	108353933
1	165483805	165483806	G	A	10	GENIC	homozygous	108353935
1	165484070	165484071	A	G	11	GENIC	homozygous	108353937
1	165484797	165484798	A	G	17	GENIC	homozygous	108353939
1	165484854	165484855	C	T	28	GENIC	homozygous	108353941
1	165484879	165484880	T	C	19	GENIC	homozygous	108353943
1	165485265	165485266	C	T	24	GENIC	homozygous	108353945
1	165485329	165485330	C	T	30	GENIC	homozygous	108353947
1	165485421	165485422	C	G	16	GENIC	homozygous	108353949
1	165485597	165485598	A	G	15	GENIC	homozygous	108353951
1	165486329	165486330	C	A	18	GENIC	homozygous	108353953
1	165486745	165486746	A	G	13	GENIC	homozygous	108353955
1	165487141	165487142	T	C	19	GENIC	homozygous	108353957
1	165488963	165488964	A	G	19	GENIC	homozygous	108353959
1	165490953	165490954	C	T	7	GENIC	heterozygous	108353960
1	165491352	165491353	C	T	13	GENIC	homozygous	108353962
1	165492011	165492012	G	A	8	GENIC	homozygous	108353964
1	165492435	165492436	C	G	14	GENIC	homozygous	108954381
1	165492543	165492544	C	T	18	GENIC	homozygous	108353966
1	165492587	165492588	A	G	11	GENIC	homozygous	108353968
1	165493529	165493530	C	T	18	GENIC	homozygous	108353970
1	165493703	165493704	T	C	11	GENIC	homozygous	108353972
1	165495417	165495418	A	G	17	GENIC	homozygous	108353974