chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	169645649	169645650	C	T	28	GENIC	homozygous	119538283
4	169773450	169773451	A	C	33	GENIC	homozygous	113406610
4	169775789	169775790	T	C	50	GENIC	homozygous	113406612
4	169778408	169778409	T	C	41	GENIC	homozygous	113406614
4	169778739	169778740	A	G	13	GENIC	homozygous	113406616
4	169778966	169778967	T	C	43	GENIC	homozygous	113406618
4	169779116	169779117	A	G	25	GENIC	homozygous	113406620
4	169797508	169797509	G	A	44	GENIC	homozygous	113406626
4	169798341	169798342	T	C	18	GENIC	homozygous	113406628
4	169798966	169798967	C	A	34	GENIC	possibly homozygous	113406630
4	169799587	169799588	C	T	39	GENIC	homozygous	113406632
4	169799820	169799821	C	T	6	GENIC	homozygous	113406634
4	169799917	169799918	A	C	27	GENIC	homozygous	113313973
4	169799963	169799964	C	T	55	GENIC	homozygous	113313974
4	169804815	169804816	G	A	32	GENIC	homozygous	113313975
4	169808853	169808854	A	G	15	GENIC	homozygous	113313977
4	169809047	169809048	T	C	55	GENIC	homozygous	113313978
4	169811111	169811112	C	T	24	GENIC	homozygous	113313980
4	169845397	169845398	G	T	12	GENIC	homozygous	112946694
4	169873955	169873956	G	A	17	GENIC	homozygous	119550857
4	169893886	169893887	C	A	20	GENIC	homozygous	112947012
4	169990682	169990683	C	T	34	GENIC	homozygous	119320453