chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11254128	11254129	A	G	45	GENIC	homozygous	115415385
12	11254594	11254595	T	C	36	GENIC	homozygous	115415391
12	11255583	11255584	A	T	34	GENIC	homozygous	115254928
12	11255601	11255602	A	G	35	GENIC	homozygous	115254930
12	11255855	11255856	C	T	41	GENIC	possibly homozygous	115415393
12	11255941	11255942	C	T	36	GENIC	homozygous	115415395
12	11255992	11255993	A	G	36	GENIC	homozygous	115254934
12	11256322	11256323	G	A	36	GENIC	homozygous	115415397
12	11256846	11256847	T	G	36	GENIC	homozygous	115254936
12	11256867	11256868	T	C	34	GENIC	homozygous	115254938
12	11257116	11257117	A	C	31	GENIC	possibly homozygous	115254942
12	11257544	11257545	A	G	35	GENIC	homozygous	115254944
12	11257550	11257551	A	G	35	GENIC	homozygous	115254946
12	11257784	11257785	G	A	19	GENIC	heterozygous	115415399
12	11258862	11258863	A	C	38	GENIC	homozygous	115361399
12	11259890	11259891	G	A	36	GENIC	homozygous	115254952
12	11260146	11260147	A	G	33	GENIC	possibly homozygous	115254954
12	11260443	11260444	A	G	32	GENIC	homozygous	115254956
12	11260606	11260607	G	A	42	GENIC	homozygous	115415403
12	11261050	11261051	C	T	44	GENIC	homozygous	115254958
12	11261096	11261097	T	C	44	GENIC	homozygous	115254960
12	11261248	11261249	G	C	44	GENIC	possibly homozygous	115415405
12	11261272	11261273	T	A	42	GENIC	possibly homozygous	115415407
12	11261273	11261274	T	A	42	GENIC	possibly homozygous	115415409
12	11261333	11261334	G	A	52	GENIC	possibly homozygous	115415412
12	11261631	11261632	A	T	34	GENIC	homozygous	115254962
12	11263127	11263128	A	T	18	GENIC	homozygous	115521329
12	11263795	11263796	T	G	19	GENIC	homozygous	115254970
12	11265052	11265053	C	A	32	GENIC	homozygous	115254980