chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26338028	26338029	A	G	55	GENIC	homozygous	115292461
12	26338111	26338112	C	A	43	GENIC	homozygous	115292463
12	26338817	26338818	C	T	52	GENIC	homozygous	115292465
12	26338930	26338931	C	T	76	GENIC	possibly homozygous	115292467
12	26339896	26339897	C	T	86	GENIC	homozygous	115292473
12	26342303	26342304	G	A	64	GENIC	homozygous	115292489
12	26338362	26338363	C	T	64	GENIC	homozygous	115621536
12	26339571	26339572	G	A	59	GENIC	homozygous	115599499
12	26342708	26342709	G	T	60	GENIC	heterozygous	118301941
12	26344578	26344579	C	A	49	GENIC	homozygous	115582097
12	26345456	26345457	G	A	48	GENIC	homozygous	115540220
12	26347490	26347491	C	T	63	GENIC	homozygous	115599501
12	26348388	26348389	A	G	73	GENIC	possibly homozygous	115540222
12	26348723	26348724	C	T	52	GENIC	homozygous	115540224
12	26348827	26348828	G	A	58	GENIC	homozygous	115540226
12	26349029	26349030	C	T	92	GENIC	heterozygous	118262805
12	26349033	26349034	C	T	94	GENIC	heterozygous	118262806
12	26349037	26349038	C	T	95	GENIC	heterozygous	118262807
12	26349053	26349054	T	C	87	GENIC	heterozygous	118262811
12	26349057	26349058	T	C	84	GENIC	heterozygous	118301942
12	26349071	26349072	T	C	87	GENIC	heterozygous	118301943
12	26349236	26349237	G	C	54	GENIC	homozygous	115540228
12	26349513	26349514	A	T	56	GENIC	homozygous	115540230
12	26349815	26349816	A	G	54	GENIC	possibly homozygous	115292505
12	26349957	26349958	C	A	38	GENIC	homozygous	115510576
12	26350036	26350037	C	A	33	GENIC	heterozygous	118301944
12	26350039	26350040	C	A	27	GENIC	possibly homozygous	118301945