chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11273021	11273022	T	C	35	GENIC	homozygous	115255058
12	11273227	11273228	C	T	46	GENIC	homozygous	115255060
12	11273556	11273557	G	A	44	GENIC	possibly homozygous	118244415
12	11273723	11273724	A	T	13	GENIC	possibly homozygous	118244416
12	11275916	11275917	G	A	3	GENIC	homozygous	118244417
12	11275921	11275922	C	T	3	GENIC	homozygous	118244418
12	11276001	11276002	C	G	6	GENIC	heterozygous	118244419
12	11276009	11276010	T	A	18	GENIC	heterozygous	118244420
12	11276013	11276014	C	T	21	GENIC	heterozygous	118244421
12	11276014	11276015	A	G	22	GENIC	heterozygous	118244422
12	11276019	11276020	C	G	26	GENIC	heterozygous	118244423
12	11276028	11276029	C	A	24	GENIC	heterozygous	118244424
12	11276037	11276038	T	A	29	GENIC	heterozygous	118244425
12	11276041	11276042	T	C	33	GENIC	heterozygous	118244426
12	11276121	11276122	T	A	22	GENIC	possibly homozygous	118244427
12	11276126	11276127	G	C	19	GENIC	homozygous	118244428
12	11276140	11276141	G	A	28	GENIC	homozygous	118244429
12	11276145	11276146	C	T	27	GENIC	heterozygous	118244430
12	11276154	11276155	A	G	28	GENIC	heterozygous	115415429
12	11276157	11276158	G	T	27	GENIC	possibly homozygous	118244431
12	11275915	11275916	C	T	3	GENIC	homozygous	115594825
12	11279065	11279066	T	G	60	GENIC	homozygous	115255062
12	11280509	11280510	T	C	32	GENIC	homozygous	115255064
12	11281392	11281393	G	T	51	GENIC	possibly homozygous	115255066
12	11283138	11283139	G	A	58	GENIC	homozygous	115255068
12	11283636	11283637	T	C	33	GENIC	homozygous	115255070
12	11283932	11283933	T	C	42	GENIC	homozygous	115255072
12	11286309	11286310	T	C	35	GENIC	homozygous	115255074
12	11289086	11289087	T	C	39	GENIC	homozygous	115466172
12	11289366	11289367	A	C	57	GENIC	homozygous	115255076
12	11290772	11290773	C	T	33	GENIC	homozygous	115255078
12	11293686	11293687	A	T	37	GENIC	homozygous	115255080
12	11293893	11293894	G	T	27	GENIC	homozygous	115255082