chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25097482	25097483	T	C	11	GENIC	homozygous	115289617
12	25098795	25098796	G	A	22	GENIC	homozygous	115289621
12	25098830	25098831	A	G	11	GENIC	homozygous	115422806
12	25101385	25101386	G	A	18	GENIC	homozygous	115369118
12	25102159	25102160	T	C	23	GENIC	homozygous	115289631
12	25102629	25102630	G	C	29	GENIC	homozygous	115289635
12	25102753	25102754	T	C	5	GENIC	homozygous	115289637
12	25104333	25104334	G	A	20	GENIC	homozygous	115369120
12	25104647	25104648	T	A	15	GENIC	homozygous	115422808
12	25104649	25104650	A	C	15	GENIC	homozygous	115422810
12	25105524	25105525	T	C	19	GENIC	homozygous	115289647
12	25105891	25105892	G	A	20	GENIC	homozygous	115369122
12	25105991	25105992	T	A	27	GENIC	homozygous	115289651
12	25106370	25106371	G	A	31	GENIC	homozygous	115369124
12	25106665	25106666	G	A	21	GENIC	homozygous	115289657
12	25106678	25106679	A	G	21	GENIC	homozygous	115369126
12	25107613	25107614	A	G	16	GENIC	homozygous	115289665
12	25107935	25107936	A	C	12	GENIC	homozygous	115369128