chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	16413640	16413641	T	C	37	GENIC	homozygous	114177240
5	16415358	16415359	A	T	58	GENIC	homozygous	114177241
5	16416373	16416374	T	C	72	GENIC	homozygous	114177242
5	16416987	16416988	G	A	40	GENIC	homozygous	114177243
5	16418066	16418067	A	G	54	GENIC	homozygous	114177244
5	16418250	16418251	G	A	44	GENIC	homozygous	114177245
5	16422511	16422512	G	C	45	GENIC	homozygous	113673520
5	16422539	16422540	C	A	44	GENIC	homozygous	113673522
5	16422545	16422546	G	A	43	GENIC	homozygous	114177246
5	16423952	16423953	G	T	41	GENIC	possibly homozygous	114177247
5	16424393	16424394	C	A	40	GENIC	homozygous	114177248
5	16424686	16424687	A	C	43	GENIC	homozygous	113673524
5	16426760	16426761	G	T	29	GENIC	possibly homozygous	114108688
5	16426833	16426834	T	G	27	GENIC	heterozygous	113673532
5	16428116	16428117	G	T	43	GENIC	heterozygous	114177249
5	16428435	16428436	A	G	46	GENIC	homozygous	113673536
5	16429870	16429871	A	G	46	GENIC	possibly homozygous	114177250
5	16431386	16431387	G	T	35	GENIC	possibly homozygous	114177251
5	16433034	16433035	G	A	40	GENIC	homozygous	114177252
5	16434248	16434249	T	C	51	GENIC	homozygous	114177253
5	16435292	16435293	A	G	88	GENIC	heterozygous	113673560
5	16435659	16435660	A	G	26	GENIC	possibly homozygous	114177256
5	16437922	16437923	T	C	55	GENIC	heterozygous	114177257
5	16437934	16437935	T	C	53	GENIC	heterozygous	114177258
5	16441279	16441280	C	T	55	GENIC	homozygous	114177259
5	16442780	16442781	T	C	27	GENIC	heterozygous	113673584
5	16443161	16443162	A	C	55	GENIC	homozygous	114177260
5	16445094	16445095	A	C	54	GENIC	homozygous	113673594
5	16437937	16437938	G	A	52	GENIC	heterozygous	114328175