chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	15445170	15445171	G	C	5	GENIC	homozygous	118201022
11	15445180	15445180		C	5	GENIC	homozygous	129987069
11	15445187	15445187		CCCC	6	GENIC	homozygous	129987071
11	15445188	15445188		TCC	6	GENIC	homozygous	129987073
11	15445204	15445204		TCTC	9	GENIC	homozygous	129987074
11	15445218	15445219	T		13	GENIC	homozygous	130399236
11	15445226	15445226		A	16	GENIC	homozygous	129987077
11	15445230	15445233	AAT		17	GENIC	homozygous	129987079
11	15445235	15445235		TG	17	GENIC	homozygous	129987080
11	15445237	15445237		T	20	GENIC	homozygous	129987082
11	15445240	15445240		T	21	GENIC	homozygous	129987083
11	15449041	15449042	G	T	18	GENIC	homozygous	118135721
11	15477832	15477833	G	C	49	GENIC	heterozygous	118176286
11	15481426	15481427	G		45	GENIC	homozygous	128885739
11	15485566	15485567	G	A	48	GENIC	homozygous	115758934
11	15485573	15485574	G	T	48	GENIC	homozygous	115758936
11	15485575	15485576	G	T	49	GENIC	homozygous	115758938
11	15520009	15520011	AG		34	GENIC	homozygous	130399237
11	15529962	15529962		TGCAGTCAAGTATGAGGAAGCAGTAGAACTTAGCAAACATGTAACACGTATGATGACCGCGGGTCAGCTTCCTTGCTCAT	46	GENIC	homozygous	128885754
11	15530051	15530052	T	A	51	GENIC	homozygous	115758998
11	15530053	15530054	G	T	51	GENIC	homozygous	115759000
11	15530081	15530082	A	C	49	GENIC	homozygous	115759002
11	15530082	15530083	C	A	49	GENIC	homozygous	115759004