chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80454336	80454337	C	CTTT	7	GENIC	heterozygous	51050728
11	80455607	80455608	G	T	14	GENIC	possibly homozygous	50969400
11	80455804	80455805	T	C	2	GENIC	heterozygous	51022069
11	80456110	80456111	A	G	26	GENIC	possibly homozygous	50969401
11	80456351	80456352	G	A	9	GENIC	homozygous	50969402
11	80457081	80457082	A	AAAAGC	3	GENIC	heterozygous	51228417
11	80457603	80457605	CG	--	5	GENIC	homozygous	50969406
11	80460321	80460322	G	A	20	GENIC	possibly homozygous	51022072
11	80462385	80462386	A	-	6	GENIC	homozygous	51022073
11	80462838	80462839	G	A	10	GENIC	homozygous	50969411
11	80463750	80463751	A	T	12	GENIC	possibly homozygous	50969412
11	80463754	80463755	A	C	9	GENIC	homozygous	50969413
11	80464620	80464621	G	A	13	GENIC	homozygous	50969414
11	80465230	80465231	C	G	14	GENIC	homozygous	50969418
11	80465348	80465349	A	G	13	GENIC	homozygous	51022074
11	80471499	80471500	T	TA	1	GENIC	homozygous	51243667
11	80476071	80476072	C	T	7	GENIC	homozygous	51022077