chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80454068	80454069	C	T	24	GENIC	homozygous	50969397
11	80455076	80455077	A	G	12	GENIC	homozygous	50969398
11	80455566	80455567	G	A	22	GENIC	homozygous	50969399
11	80455607	80455608	G	T	23	GENIC	homozygous	50969400
11	80456110	80456111	A	G	22	GENIC	homozygous	50969401
11	80456351	80456352	G	A	17	GENIC	homozygous	50969402
11	80457085	80457086	A	G	20	GENIC	homozygous	50969403
11	80457131	80457132	A	C	20	GENIC	homozygous	50969404
11	80457131	80457132	A	AC	17	GENIC	possibly homozygous	50969405
11	80457603	80457605	CG	--	19	GENIC	homozygous	50969406
11	80457786	80457790	GGGG	----	9	GENIC	possibly homozygous	50969407
11	80457787	80457790	GGG	---	9	GENIC	heterozygous	50969408
11	80457982	80457983	T	TCC	2	GENIC	homozygous	50969409
11	80458720	80458724	AAAC	----	14	GENIC	homozygous	50969410
11	80462838	80462839	G	A	18	GENIC	homozygous	50969411
11	80463750	80463751	A	T	27	GENIC	homozygous	50969412
11	80463754	80463755	A	C	28	GENIC	homozygous	50969413
11	80464620	80464621	G	A	25	GENIC	homozygous	50969414
11	80465140	80465141	G	C	21	GENIC	possibly homozygous	50969415
11	80465142	80465143	G	C	21	GENIC	possibly homozygous	50969416
11	80465144	80465145	G	C	20	GENIC	possibly homozygous	50969417
11	80465230	80465231	C	G	20	GENIC	possibly homozygous	50969418
11	80466848	80466849	T	TA	16	GENIC	homozygous	50969419
11	80467914	80467915	C	T	23	GENIC	homozygous	50969420
11	80468517	80468518	G	C	24	GENIC	homozygous	50969421
11	80469925	80469928	TTT	---	16	GENIC	homozygous	50969422
11	80471500	80471501	A	-	1	GENIC	homozygous	50969423
11	80472336	80472337	G	A	25	GENIC	homozygous	50969424
11	80474148	80474150	TT	--	16	GENIC	heterozygous	50969425
11	80474149	80474150	T	-	16	GENIC	heterozygous	50842444
11	80474953	80474954	T	TACAC	5	GENIC	homozygous	50969426
11	80475723	80475724	C	A	16	GENIC	homozygous	50969427