chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	208003523	208003524	T	-	24	GENIC	homozygous	59356885
2	208004047	208004051	GTGT	----	10	GENIC	heterozygous	59771509
2	208004220	208004224	CTCT	----	26	GENIC	homozygous	59356886
2	208004312	208004313	T	G	9	GENIC	heterozygous	59356887
2	208004316	208004317	A	G	11	GENIC	heterozygous	59356888
2	208004332	208004333	T	C	11	GENIC	heterozygous	59356889
2	208004889	208004890	C	CA	19	GENIC	heterozygous	59356890
2	208004898	208004899	A	T	30	GENIC	heterozygous	59771510
2	208004906	208004907	T	TAAATA	18	GENIC	homozygous	59356891
2	208005192	208005193	T	C	34	GENIC	homozygous	59356892
2	208005434	208005435	A	G	49	GENIC	homozygous	59356893
2	208005444	208005445	C	G	52	GENIC	homozygous	59356894
2	208005978	208005981	GAG	---	32	GENIC	homozygous	59356895
2	208006858	208006859	G	-	52	GENIC	homozygous	59356896
2	208006920	208006921	T	C	63	GENIC	homozygous	59356897
2	208007097	208007098	T	TC	42	GENIC	homozygous	59356898
2	208007458	208007459	G	-	51	GENIC	homozygous	59356899
2	208008550	208008551	C	T	45	GENIC	homozygous	59356900
2	208008974	208008975	C	T	43	GENIC	homozygous	59356901
2	208009641	208009642	C	A	41	GENIC	possibly homozygous	59356902
2	208009696	208009697	G	A	39	GENIC	homozygous	59356903