chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80454068	80454069	C	T	19	GENIC	heterozygous	50969397
11	80455076	80455077	A	G	18	GENIC	heterozygous	50969398
11	80455566	80455567	G	A	19	GENIC	heterozygous	50969399
11	80455607	80455608	G	T	17	GENIC	homozygous	50969400
11	80456110	80456111	A	G	21	GENIC	homozygous	50969401
11	80456351	80456352	G	A	14	GENIC	homozygous	50969402
11	80457131	80457132	A	C	11	GENIC	heterozygous	50969404
11	80460321	80460322	G	A	23	GENIC	heterozygous	51022072
11	80462385	80462386	A	-	11	GENIC	heterozygous	51022073
11	80462838	80462839	G	A	11	GENIC	homozygous	50969411
11	80463750	80463751	A	T	17	GENIC	homozygous	50969412
11	80463754	80463755	A	C	18	GENIC	homozygous	50969413
11	80464620	80464621	G	A	15	GENIC	homozygous	50969414
11	80465230	80465231	C	G	11	GENIC	homozygous	50969418
11	80465348	80465349	A	G	14	GENIC	heterozygous	51022074
11	80468517	80468518	G	C	14	GENIC	heterozygous	50969421
11	80472336	80472337	G	A	11	GENIC	heterozygous	50969424
11	80475723	80475724	C	A	14	GENIC	heterozygous	50969427