chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	25222897	25222898	G	A	32	GENIC	homozygous	110491628
2	25223520	25223521	C	T	43	GENIC	homozygous	110491630
2	25223711	25223712	A	G	35	GENIC	possibly homozygous	110491632
2	25223754	25223755	G	A	49	GENIC	possibly homozygous	110491634
2	25223757	25223758	G	A	51	GENIC	possibly homozygous	110491636
2	25223891	25223892	T	C	19	GENIC	homozygous	110491638
2	25223901	25223902	T	C	20	GENIC	heterozygous	110491640
2	25223926	25223927	G	T	38	GENIC	heterozygous	110491642
2	25223935	25223936	G	T	45	GENIC	heterozygous	110491644
2	25223944	25223945	T	G	47	GENIC	heterozygous	110491646
2	25223953	25223954	C	G	44	GENIC	heterozygous	110491648
2	25223998	25223999	T	C	65	GENIC	homozygous	110491650
2	25225888	25225889	C	T	62	GENIC	homozygous	110491652
2	25227222	25227223	C	G	56	GENIC	homozygous	110491654
2	25228323	25228324	A	G	58	GENIC	homozygous	110491655
2	25229659	25229660	C	T	56	GENIC	homozygous	110491657
2	25230752	25230753	C	T	77	GENIC	homozygous	110491659
2	25231431	25231432	C	T	50	GENIC	homozygous	110491661
2	25232725	25232726	A	G	40	GENIC	homozygous	110491663
2	25234251	25234252	T	A	64	GENIC	homozygous	110491665
2	25234405	25234406	T	C	39	GENIC	homozygous	110491667
2	25234421	25234422	A	C	38	GENIC	homozygous	110491669