chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2558577	2558578	A	G	39	GENIC	homozygous	115234672
12	2560124	2560125	G	A	22	GENIC	homozygous	115357478
12	2560637	2560638	T	A	37	GENIC	homozygous	115357479
12	2560858	2560859	C	T	21	GENIC	homozygous	118235213
12	2560978	2560979	T	G	18	GENIC	possibly homozygous	115521012
12	2561594	2561595	T	G	15	GENIC	homozygous	115357480
12	2561660	2561661	A	G	12	GENIC	homozygous	115490651
12	2561661	2561662	A	T	12	GENIC	homozygous	115490654
12	2562270	2562271	T	C	9	GENIC	homozygous	115234678
12	2563742	2563743	A	G	24	GENIC	homozygous	115357481
12	2564622	2564623	A	G	19	GENIC	homozygous	115234683
12	2566165	2566166	A	G	26	GENIC	homozygous	115234687
12	2566558	2566559	A	G	39	GENIC	possibly homozygous	115234689
12	2566998	2566999	T	G	31	GENIC	homozygous	115234691
12	2567115	2567116	T	C	24	GENIC	homozygous	115234693
12	2567663	2567664	G	C	28	GENIC	homozygous	115234695
12	2567748	2567749	G	A	15	GENIC	homozygous	115234697
12	2561704	2561705	C	T	24	GENIC	heterozygous	115701747