chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230302912	230302913	G	T	27	GENIC	homozygous	74936780
2	230303065	230303066	G	T	32	GENIC	homozygous	75571530
2	230303066	230303067	T	C	32	GENIC	homozygous	75571532
2	230303165	230303166	A	T	29	GENIC	homozygous	74936781
2	230303246	230303247	G	A	28	GENIC	possibly homozygous	74936782
2	230303717	230303718	A	G	13	GENIC	homozygous	74936783
2	230303788	230303789	G	A	22	GENIC	possibly homozygous	74936784
2	230303796	230303797	G	A	22	GENIC	homozygous	74936785
2	230303810	230303811	G	A	24	GENIC	homozygous	74936786
2	230304889	230304890	A	G	24	GENIC	homozygous	74936788
2	230305761	230305762	G	A	11	GENIC	homozygous	74936790
2	230305937	230305938	A	G	23	GENIC	homozygous	74441416
2	230305193	230305194	T	C	20	GENIC	possibly homozygous	74441414
2	230306437	230306438	G	A	16	GENIC	possibly homozygous	74936791
2	230306825	230306826	C	A	27	GENIC	homozygous	74936792
2	230306845	230306846	G	A	29	GENIC	homozygous	74936793
2	230307170	230307171	A	G	25	GENIC	homozygous	74936794
2	230307240	230307241	C	T	20	GENIC	possibly homozygous	74936795
2	230307310	230307311	T	C	16	GENIC	homozygous	74441418
2	230307649	230307650	G	A	25	GENIC	homozygous	74936796