chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30880255	30880256	C	T	92	GENIC	heterozygous	118141343
11	30880650	30880651	A	G	35	GENIC	homozygous	115809846
11	30881150	30881151	C	T	54	GENIC	homozygous	115809848
11	30881388	30881389	T	C	52	GENIC	homozygous	115809850
11	30883216	30883217	T	C	56	GENIC	homozygous	115809852
11	30883732	30883733	T	G	43	GENIC	possibly homozygous	118141344
11	30882936	30882937	T	C	38	GENIC	heterozygous	115959986
11	30883314	30883315	G	C	44	GENIC	homozygous	116096117
11	30884486	30884487	A	G	72	GENIC	homozygous	115809854
11	30885831	30885832	C	T	76	GENIC	homozygous	115809856
11	30886157	30886158	C	T	40	GENIC	homozygous	115809858
11	30886629	30886630	A	G	74	GENIC	possibly homozygous	115809860
11	30886795	30886796	T	C	49	GENIC	homozygous	116243527
11	30887179	30887180	T	C	62	GENIC	homozygous	115809862
11	30887257	30887258	G	A	41	GENIC	homozygous	115809864
11	30889480	30889481	A	G	65	GENIC	homozygous	115809866
11	30889600	30889601	C	T	69	GENIC	homozygous	115809868
11	30889986	30889987	A	G	41	GENIC	possibly homozygous	116096129
11	30890081	30890082	T	G	35	GENIC	homozygous	115809872
11	30892838	30892839	T	C	35	GENIC	homozygous	115809874