chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25097482	25097483	T	C	27	GENIC	homozygous	115289617
12	25098795	25098796	G	A	48	GENIC	homozygous	115289621
12	25101275	25101276	T		57	GENIC	possibly homozygous	128974063
12	25102159	25102160	T	C	43	GENIC	homozygous	115289631
12	25102629	25102630	G	C	50	GENIC	homozygous	115289635
12	25102753	25102754	T	C	51	GENIC	homozygous	115289637
12	25103232	25103233	G	T	10	GENIC	homozygous	115505445
12	25104649	25104650	A	C	48	GENIC	homozygous	115422810
12	25098830	25098831	A	G	35	GENIC	homozygous	115422806
12	25104647	25104648	T	A	48	GENIC	homozygous	115422808
12	25101385	25101386	G	A	49	GENIC	homozygous	115369118
12	25104333	25104334	G	A	56	GENIC	homozygous	115369120
12	25103280	25103280		T	19	GENIC	possibly homozygous	131115636
12	25103433	25103437	ATAG		53	GENIC	homozygous	131115637
12	25105524	25105525	T	C	54	GENIC	homozygous	115289647
12	25105891	25105892	G	A	45	GENIC	homozygous	115369122
12	25105991	25105992	T	A	48	GENIC	homozygous	115289651
12	25106370	25106371	G	A	44	GENIC	homozygous	115369124
12	25106636	25106636		AAAG	39	GENIC	homozygous	128974070
12	25106665	25106666	G	A	35	GENIC	homozygous	115289657
12	25106674	25106674		GTGG	32	GENIC	possibly homozygous	128974071
12	25106678	25106679	A	G	36	GENIC	homozygous	115369126
12	25107613	25107614	A	G	50	GENIC	homozygous	115289665
12	25107760	25107761	T	C	19	GENIC	homozygous	131916764
12	25107780	25107781	G	A	26	GENIC	homozygous	118262442
12	25108808	25108809	A		45	GENIC	homozygous	131115638
12	25107935	25107936	A	C	42	GENIC	homozygous	115369128