chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89200001	89200002	G	A	38	GENIC	homozygous	116819638
10	89201640	89201641	C	T	30	GENIC	homozygous	116819640
10	89202617	89202618	C	T	14	GENIC	homozygous	116819642
10	89203830	89203831	T	A	16	GENIC	homozygous	116819644
10	89203831	89203832	T	A	16	GENIC	homozygous	116819646
10	89204401	89204402	A	C	26	GENIC	homozygous	116819648
10	89204714	89204715	C	T	31	GENIC	homozygous	116819650
10	89204974	89204975	T	C	26	GENIC	homozygous	116819652
10	89205733	89205734	A	G	39	GENIC	homozygous	116819654
10	89206109	89206110	C	T	54	GENIC	homozygous	116819656
10	89206617	89206618	T	A	21	GENIC	homozygous	116819658
10	89207830	89207831	A	G	43	GENIC	homozygous	116675226
10	89208584	89208585	C	T	29	GENIC	homozygous	116819660
10	89209357	89209358	G	A	13	GENIC	homozygous	116819662
10	89210084	89210085	T	G	33	GENIC	homozygous	116819664