chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80454068	80454069	C	T	22	GENIC	homozygous	50969397
11	80455076	80455077	A	G	16	GENIC	possibly homozygous	50969398
11	80455566	80455567	G	A	19	GENIC	possibly homozygous	50969399
11	80455607	80455608	G	T	23	GENIC	possibly homozygous	50969400
11	80456110	80456111	A	G	28	GENIC	possibly homozygous	50969401
11	80456351	80456352	G	A	21	GENIC	homozygous	50969402
11	80457085	80457086	A	G	3	GENIC	homozygous	50969403
11	80457603	80457605	CG	--	8	GENIC	homozygous	50969406
11	80458720	80458724	AAAC	----	5	GENIC	homozygous	50969410
11	80462385	80462386	A	-	6	GENIC	heterozygous	51022073
11	80462838	80462839	G	A	8	GENIC	homozygous	50969411
11	80463750	80463751	A	T	7	GENIC	homozygous	50969412
11	80463754	80463755	A	C	8	GENIC	homozygous	50969413
11	80464620	80464621	G	A	20	GENIC	homozygous	50969414
11	80465230	80465231	C	G	20	GENIC	homozygous	50969418
11	80467914	80467915	C	T	21	GENIC	possibly homozygous	50969420
11	80468517	80468518	G	C	15	GENIC	homozygous	50969421
11	80472336	80472337	G	A	13	GENIC	homozygous	50969424
11	80475723	80475724	C	A	8	GENIC	homozygous	50969427