chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11233895	11233896	T	C	35	GENIC	homozygous	115415328
12	11233954	11233955	T	C	32	GENIC	homozygous	115415330
12	11234299	11234300	C	T	42	GENIC	homozygous	115254904
12	11234749	11234750	G	A	29	GENIC	homozygous	115415332
12	11234876	11234877	G	A	26	GENIC	homozygous	115415334
12	11235879	11235880	A	T	20	GENIC	homozygous	115254906
12	11235903	11235904	T	C	17	GENIC	homozygous	115254908
12	11236578	11236579	C	T	33	GENIC	homozygous	115415336
12	11236915	11236916	A	G	26	GENIC	homozygous	115415338
12	11237032	11237033	G	A	29	GENIC	homozygous	115415340
12	11237372	11237373	T	C	50	GENIC	homozygous	115415342
12	11237673	11237674	G	T	21	GENIC	homozygous	115415344
12	11238630	11238631	G	T	33	GENIC	homozygous	115415346
12	11239311	11239312	G	A	18	GENIC	homozygous	118335675
12	11236478	11236479	T	C	43	GENIC	heterozygous	115482335
12	11236487	11236488	G	A	42	GENIC	heterozygous	115482336
12	11236488	11236489	T	C	40	GENIC	heterozygous	115482337