chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	27008067	27008068	T	C	37	GENIC	homozygous	115798689
11	27008459	27008460	A	C	19	GENIC	homozygous	115798691
11	27008975	27008976	T	C	27	GENIC	homozygous	115798693
11	27009413	27009414	A	G	27	GENIC	homozygous	115798695
11	27009733	27009734	T	C	20	GENIC	homozygous	115798697
11	27010353	27010354	C	T	29	GENIC	homozygous	115798699
11	27010702	27010703	A	C	23	GENIC	homozygous	115798701
11	27011168	27011169	G	A	16	GENIC	homozygous	115956429
11	27011806	27011807	G	A	27	GENIC	homozygous	115798703
11	27012402	27012403	A	G	17	GENIC	homozygous	115798705
11	27012725	27012726	C	T	29	GENIC	homozygous	115798707
11	27012869	27012870	G	A	28	GENIC	homozygous	115798709
11	27013357	27013358	A	G	19	GENIC	homozygous	115798711
11	27013900	27013901	A	G	26	GENIC	homozygous	115798713
11	27014860	27014861	A	G	29	GENIC	homozygous	115798715
11	27016376	27016377	T	C	22	GENIC	homozygous	115798723
11	27015319	27015320	G	A	14	GENIC	homozygous	115798717
11	27015552	27015553	C	G	11	GENIC	homozygous	115798719
11	27016674	27016675	G	C	17	GENIC	homozygous	115798725