chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	27130571	27130571		GGTTT	42	GENIC	homozygous	128893475
11	27131115	27131116	G		35	GENIC	heterozygous	128893477
11	27135208	27135209	A	G	43	GENIC	homozygous	115799147
11	27135354	27135355	A	C	45	GENIC	homozygous	115799149
11	27136465	27136465		G	43	GENIC	homozygous	128893478
11	27131776	27131777	C	T	44	GENIC	homozygous	115956499
11	27131926	27131927	T	G	52	GENIC	homozygous	115956500
11	27132722	27132723	C	T	46	GENIC	homozygous	115956501
11	27133152	27133153	G	C	42	GENIC	homozygous	115956502
11	27133586	27133587	C	T	38	GENIC	homozygous	115956503
11	27136660	27136661	T	A	39	GENIC	homozygous	115956504
11	27137293	27137294	A	G	43	GENIC	homozygous	115799151
11	27137625	27137626	G	T	35	GENIC	homozygous	115799153
11	27138421	27138422	C	T	44	GENIC	possibly homozygous	115956505
11	27138604	27138605	C	T	46	GENIC	homozygous	115956506
11	27139725	27139726	A	C	41	GENIC	homozygous	115799155
11	27139767	27139768	T	C	44	GENIC	homozygous	115956507
11	27141371	27141372	C	T	39	GENIC	homozygous	115799159
11	27138257	27138258	C		35	GENIC	homozygous	131103800
11	27141054	27141057	AAT		34	GENIC	homozygous	131103801
11	27141880	27141881	A	T	45	GENIC	homozygous	116095089