chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80454336	80454337	C	CTTT	16	GENIC	homozygous	51050728
11	80455607	80455608	G	T	31	GENIC	homozygous	50969400
11	80456110	80456111	A	G	22	GENIC	homozygous	50969401
11	80456351	80456352	G	A	25	GENIC	homozygous	50969402
11	80456976	80456977	A	G	25	GENIC	homozygous	51050730
11	80457085	80457086	A	G	20	GENIC	heterozygous	50969403
11	80457096	80457097	C	CA	20	GENIC	heterozygous	51050732
11	80457131	80457132	A	AC	24	GENIC	possibly homozygous	50969405
11	80457331	80457332	G	C	18	GENIC	heterozygous	51022071
11	80457787	80457790	GGG	---	9	GENIC	heterozygous	50969408
11	80457983	80457984	C	-	29	GENIC	homozygous	51050734
11	80458964	80458965	G	A	47	GENIC	homozygous	51050736
11	80459919	80459920	T	C	39	GENIC	homozygous	51050737
11	80460321	80460322	G	A	29	GENIC	homozygous	51022072
11	80462384	80462385	T	TA	24	GENIC	homozygous	51050739
11	80462838	80462839	G	A	36	GENIC	homozygous	50969411
11	80462961	80462969	GTCGAGAG	--------	22	GENIC	homozygous	51050741
11	80463750	80463751	A	T	30	GENIC	homozygous	50969412
11	80463754	80463755	A	C	27	GENIC	homozygous	50969413
11	80463926	80463927	G	C	30	GENIC	homozygous	51050743
11	80464403	80464404	T	C	39	GENIC	homozygous	51050744
11	80464620	80464621	G	A	40	GENIC	homozygous	50969414
11	80465029	80465033	TCTG	----	26	GENIC	homozygous	51050746
11	80465230	80465231	C	G	31	GENIC	homozygous	50969418
11	80467124	80467125	T	TCA	7	GENIC	possibly homozygous	51050748
11	80469333	80469334	C	T	22	GENIC	homozygous	51050750
11	80469926	80469928	TT	--	12	GENIC	heterozygous	51050752
11	80470957	80470958	G	A	20	GENIC	homozygous	51050753
11	80471500	80471501	A	-	2	GENIC	homozygous	50969423
11	80469925	80469928	TTT	---	12	GENIC	heterozygous	50969422
11	80472196	80472197	C	T	10	GENIC	homozygous	51050755
11	80473538	80473539	C	T	29	GENIC	homozygous	51050757
11	80474007	80474009	AA	--	25	GENIC	homozygous	51022075
11	80474148	80474150	TT	--	24	GENIC	homozygous	50969425
11	80474953	80474954	T	TACAC	4	GENIC	homozygous	50969426