chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	179803390	179803391	C	T	16	GENIC	homozygous	58264260
3	179803505	179803506	G	A	8	GENIC	homozygous	58264262
3	179804063	179804064	A	G	14	GENIC	homozygous	58264264
3	179804075	179804076	G	A	14	GENIC	homozygous	58264266
3	179804264	179804265	T	C	11	GENIC	homozygous	58264268
3	179804417	179804418	T	TCACTCA	8	GENIC	homozygous	57817875
3	179804719	179804720	T	C	11	GENIC	homozygous	58264270
3	179804759	179804760	A	G	12	GENIC	homozygous	58264272
3	179805519	179805520	A	G	16	GENIC	homozygous	58264274
3	179805765	179805766	T	A	9	GENIC	homozygous	58264276
3	179805808	179805809	G	A	12	GENIC	homozygous	58264278
3	179806370	179806371	A	G	12	GENIC	homozygous	58264280
3	179806810	179806811	G	A	16	GENIC	homozygous	58264282
3	179808187	179808188	T	C	9	GENIC	homozygous	58264284
3	179808196	179808197	C	A	9	GENIC	homozygous	58264286
3	179809276	179809277	T	G	8	GENIC	homozygous	58264290
3	179809611	179809612	A	T	9	GENIC	homozygous	58264294
3	179810565	179810566	C	CT	10	GENIC	homozygous	58264296
3	179812247	179812248	G	A	10	GENIC	homozygous	58264302
3	179812807	179812808	C	T	11	GENIC	homozygous	58264304
3	179816625	179816626	C	T	21	GENIC	homozygous	58264306
3	179816817	179816818	T	TCC	10	GENIC	homozygous	58661299
3	179819949	179819950	T	A	9	GENIC	homozygous	58264310
3	179820263	179820264	G	A	10	GENIC	homozygous	58264312
3	179820347	179820348	A	G	11	GENIC	homozygous	58264314
3	179822802	179822803	T	TG	12	GENIC	homozygous	58264319
3	179823056	179823057	A	C	8	GENIC	homozygous	58264321
3	179823608	179823609	A	AG	18	GENIC	homozygous	57817881
3	179823612	179823613	A	-	18	GENIC	homozygous	57817883
3	179823848	179823855	TTGATGT	-------	9	GENIC	homozygous	58264325
3	179824244	179824245	T	C	8	GENIC	homozygous	58264331
3	179825497	179825498	A	C	21	GENIC	homozygous	58264333