chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80455607	80455608	G	T	27	GENIC	homozygous	50969400
11	80455804	80455805	T	C	9	GENIC	possibly homozygous	51022069
11	80456110	80456111	A	G	19	GENIC	possibly homozygous	50969401
11	80456351	80456352	G	A	13	GENIC	homozygous	50969402
11	80457321	80457322	T	TCCCCC	1	GENIC	homozygous	51170336
11	80457603	80457605	CG	--	16	GENIC	homozygous	50969406
11	80460321	80460322	G	A	23	GENIC	homozygous	51022072
11	80462385	80462386	A	-	8	GENIC	homozygous	51022073
11	80462838	80462839	G	A	8	GENIC	homozygous	50969411
11	80463750	80463751	A	T	11	GENIC	homozygous	50969412
11	80463754	80463755	A	C	12	GENIC	homozygous	50969413
11	80464620	80464621	G	A	22	GENIC	possibly homozygous	50969414
11	80465230	80465231	C	G	12	GENIC	possibly homozygous	50969418
11	80465348	80465349	A	G	20	GENIC	possibly homozygous	51022074
11	80476071	80476072	C	T	4	GENIC	heterozygous	51022077