chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	89491606	89491607	A	T	8	GENIC	homozygous	109905045
2	89491803	89491804	T	C	12	GENIC	homozygous	109905047
2	89491859	89491860	A	T	16	GENIC	homozygous	109905049
2	89492077	89492078	A	G	40	GENIC	homozygous	109905051
2	89494768	89494769	A	G	9	GENIC	homozygous	109905053
2	89495157	89495158	G	T	19	GENIC	homozygous	109905055
2	89495401	89495402	T	G	24	GENIC	homozygous	109905057
2	89495573	89495574	A	G	20	GENIC	possibly homozygous	109905059
2	89495577	89495578	G	A	20	GENIC	possibly homozygous	109905061
2	89495582	89495583	G	A	20	GENIC	homozygous	109905063
2	89496358	89496359	C	A	17	GENIC	homozygous	109905065
2	89496511	89496512	T	A	18	GENIC	homozygous	109905067
2	89496969	89496970	T	C	27	GENIC	homozygous	109905069
2	89497250	89497251	A	G	17	GENIC	homozygous	109905071
2	89497774	89497775	T	C	13	GENIC	homozygous	109905073