chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11255583	11255584	A	T	12	GENIC	homozygous	115254928
12	11255601	11255602	A	G	12	GENIC	homozygous	115254930
12	11255634	11255635	T	C	14	GENIC	possibly homozygous	115254932
12	11255992	11255993	A	G	9	GENIC	homozygous	115254934
12	11256122	11256123	G	A	11	GENIC	homozygous	115361398
12	11257116	11257117	A	C	12	GENIC	homozygous	115254942
12	11257544	11257545	A	G	6	GENIC	homozygous	115254944
12	11257550	11257551	A	G	5	GENIC	homozygous	115254946
12	11258521	11258522	C	T	11	GENIC	homozygous	115254948
12	11258862	11258863	A	C	7	GENIC	homozygous	115361399
12	11259866	11259867	C	A	7	GENIC	homozygous	115254950
12	11259890	11259891	G	A	10	GENIC	homozygous	115254952
12	11260146	11260147	A	G	6	GENIC	homozygous	115254954
12	11260443	11260444	A	G	5	GENIC	homozygous	115254956
12	11261050	11261051	C	T	9	GENIC	homozygous	115254958
12	11261096	11261097	T	C	16	GENIC	homozygous	115254960
12	11261631	11261632	A	T	7	GENIC	homozygous	115254962
12	11262479	11262480	G	A	9	GENIC	homozygous	115254964
12	11263702	11263703	T	C	6	GENIC	homozygous	115254966
12	11263708	11263709	T	A	6	GENIC	homozygous	115254968
12	11263795	11263796	T	G	6	GENIC	homozygous	115254970
12	11264110	11264111	C	T	8	GENIC	homozygous	115254972
12	11264336	11264337	G	A	10	GENIC	homozygous	115254974
12	11264386	11264387	G	C	13	GENIC	homozygous	115254976