chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	58362317	58362318	C	T	21	GENIC	homozygous	118842948
5	58363505	58363506	T	C	29	GENIC	homozygous	113818050
5	58364025	58364026	C	T	57	GENIC	homozygous	113818052
5	58364118	58364119	G	A	36	GENIC	homozygous	113818054
5	58366994	58366995	G	A	33	GENIC	homozygous	113818062
5	58367650	58367651	C	T	52	GENIC	homozygous	113818064
5	58367800	58367801	C	T	50	GENIC	homozygous	113818066
5	58367886	58367887	T	G	28	GENIC	homozygous	113818068
5	58367914	58367915	C	T	34	GENIC	homozygous	113818070
5	58367990	58367991	T	G	31	GENIC	homozygous	113818072
5	58368320	58368321	A	G	22	GENIC	homozygous	113818074
5	58369072	58369073	G	A	35	GENIC	homozygous	113818078
5	58369268	58369269	C	A	27	GENIC	homozygous	113818081
5	58369393	58369394	C	T	21	GENIC	homozygous	118842949
5	58369685	58369686	C	A	42	GENIC	homozygous	113818083
5	58370099	58370100	G	C	35	GENIC	homozygous	113818085
5	58372979	58372980	A	G	32	GENIC	possibly homozygous	113818089
5	58373059	58373060	G	A	34	GENIC	homozygous	113818090
5	58373606	58373607	A	T	56	GENIC	homozygous	113818092
5	58373866	58373867	G	A	37	GENIC	homozygous	113818094
5	58374157	58374158	T	C	41	GENIC	homozygous	113818096
5	58376139	58376140	T	C	44	GENIC	homozygous	113818098
5	58376225	58376226	A	G	52	GENIC	homozygous	113818100
5	58378775	58378776	T	C	39	GENIC	homozygous	113818104
5	58378987	58378988	A	G	54	GENIC	homozygous	113818105
5	58379998	58379999	T	C	52	GENIC	homozygous	113818107
5	58380206	58380207	T	G	33	GENIC	homozygous	113818109
5	58380632	58380633	C	T	29	GENIC	homozygous	113818111
5	58382286	58382287	G	A	34	GENIC	homozygous	113818113
5	58382695	58382696	G	A	48	GENIC	homozygous	113818115
5	58383285	58383286	A	G	33	GENIC	homozygous	113818117
5	58387010	58387011	G	A	45	GENIC	homozygous	113818119