chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89511408	89511409	T	C	10	GENIC	homozygous	116902691
10	89511450	89511451	T	C	12	GENIC	homozygous	116820211
10	89511459	89511460	G	T	13	GENIC	homozygous	116902693
10	89512360	89512361	A	G	20	GENIC	homozygous	116902695
10	89512659	89512660	G	A	14	GENIC	homozygous	116950580
10	89512705	89512706	T	C	15	GENIC	homozygous	116902697
10	89512785	89512786	T	A	19	GENIC	homozygous	116902699
10	89512835	89512836	C	T	29	GENIC	homozygous	116902701
10	89513007	89513008	T	C	22	GENIC	homozygous	116902703
10	89513072	89513073	C	T	29	GENIC	homozygous	116902705
10	89514060	89514061	G	A	23	GENIC	homozygous	116902707
10	89514110	89514111	G	A	23	GENIC	homozygous	116902709
10	89515316	89515317	C	A	16	GENIC	homozygous	116902711
10	89515474	89515475	G	T	15	GENIC	possibly homozygous	116902713
10	89516736	89516737	G	T	7	GENIC	homozygous	117068467
10	89517153	89517154	T	G	8	GENIC	homozygous	116902717
10	89517737	89517738	G	A	29	GENIC	homozygous	116902719
10	89519580	89519581	G	A	20	GENIC	homozygous	116902721
10	89520009	89520010	G	A	8	GENIC	homozygous	116902723
10	89522953	89522954	G	A	23	GENIC	homozygous	116675647
10	89524356	89524357	A	C	20	GENIC	homozygous	116675653
10	89525628	89525629	G	A	27	GENIC	homozygous	116902725
10	89526147	89526148	A	G	12	GENIC	homozygous	116675661