chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89200001	89200002	G	A	37	GENIC	homozygous	116819638
10	89200514	89200515	C	T	14	GENIC	homozygous	118048811
10	89200523	89200524	C	G	15	GENIC	homozygous	118048812
10	89202617	89202618	C	T	32	GENIC	homozygous	116819642
10	89203695	89203696	C	T	26	GENIC	homozygous	116902228
10	89203830	89203831	T	A	15	GENIC	homozygous	116819644
10	89204401	89204402	A	C	22	GENIC	homozygous	116819648
10	89204714	89204715	C	T	30	GENIC	homozygous	116819650
10	89204974	89204975	T	C	35	GENIC	homozygous	116819652
10	89205733	89205734	A	G	34	GENIC	homozygous	116819654
10	89206109	89206110	C	T	28	GENIC	possibly homozygous	116819656
10	89206617	89206618	T	A	35	GENIC	homozygous	116819658
10	89206750	89206751	C	T	24	GENIC	heterozygous	118048813
10	89207632	89207633	C	G	20	GENIC	possibly homozygous	116902230
10	89210084	89210085	T	G	22	GENIC	homozygous	116819664
10	89207830	89207831	A	G	41	GENIC	homozygous	116675226