chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	27004772	27004773	C	T	6	GENIC	homozygous	115798679
11	27005830	27005831	G	A	24	GENIC	homozygous	115798681
11	27006289	27006290	C	T	34	GENIC	homozygous	115798683
11	27007267	27007268	C	G	24	GENIC	homozygous	115798685
11	27008056	27008057	G	A	18	GENIC	homozygous	115798687
11	27008067	27008068	T	C	18	GENIC	homozygous	115798689
11	27008459	27008460	A	C	17	GENIC	homozygous	115798691
11	27008975	27008976	T	C	39	GENIC	homozygous	115798693
11	27009413	27009414	A	G	28	GENIC	homozygous	115798695
11	27009733	27009734	T	C	31	GENIC	homozygous	115798697
11	27010353	27010354	C	T	36	GENIC	homozygous	115798699
11	27010702	27010703	A	C	16	GENIC	homozygous	115798701
11	27011806	27011807	G	A	31	GENIC	homozygous	115798703
11	27012402	27012403	A	G	22	GENIC	homozygous	115798705
11	27012725	27012726	C	T	18	GENIC	homozygous	115798707
11	27012869	27012870	G	A	19	GENIC	homozygous	115798709
11	27013357	27013358	A	G	30	GENIC	homozygous	115798711
11	27013900	27013901	A	G	17	GENIC	homozygous	115798713
11	27014860	27014861	A	G	27	GENIC	homozygous	115798715
11	27015319	27015320	G	A	22	GENIC	homozygous	115798717
11	27015552	27015553	C	G	4	GENIC	homozygous	115798719
11	27016084	27016085	C	T	9	GENIC	homozygous	115956430
11	27016097	27016098	T	G	8	GENIC	homozygous	115798721
11	27016099	27016100	G	C	9	GENIC	homozygous	115956431
11	27016376	27016377	T	C	26	GENIC	homozygous	115798723
11	27016674	27016675	G	C	17	GENIC	homozygous	115798725