chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	89584770	89584771	A	T	25	GENIC	homozygous	111141063
17	89584904	89584905	C	T	22	GENIC	homozygous	111141064
17	89585661	89585662	T	G	12	GENIC	homozygous	111141066
17	89586486	89586487	A	G	41	GENIC	homozygous	111141068
17	89586763	89586764	C	G	51	GENIC	homozygous	111141070
17	89593831	89593832	C	T	26	GENIC	homozygous	111141072
17	89600771	89600772	C	T	22	GENIC	homozygous	111141074
17	89601097	89601098	G	A	30	GENIC	homozygous	111141076
17	89601163	89601164	A	T	34	GENIC	homozygous	111141078
17	89604449	89604450	T	C	41	GENIC	homozygous	111141080
17	89605068	89605069	C	T	27	GENIC	homozygous	111141082
17	89605609	89605610	T	C	20	GENIC	homozygous	111141084
17	89620553	89620554	C	A	30	GENIC	homozygous	111141086
17	89621414	89621415	A	G	27	GENIC	homozygous	111141088
17	89622409	89622410	A	G	41	GENIC	homozygous	111141090
17	89622518	89622519	G	A	35	GENIC	homozygous	111141092
17	89626215	89626216	G	T	33	GENIC	homozygous	111141094
17	89627908	89627909	C	G	29	GENIC	homozygous	111141096
17	89629944	89629945	C	T	14	GENIC	homozygous	111141098
17	89630616	89630617	G	A	24	GENIC	homozygous	111141100
17	89633711	89633712	C	T	24	GENIC	homozygous	111141101
17	89635624	89635625	C	T	40	GENIC	possibly homozygous	111141103
17	89638067	89638068	T	C	31	GENIC	homozygous	111141105
17	89640429	89640430	C	T	39	GENIC	homozygous	111141107
17	89648054	89648055	A	G	55	GENIC	homozygous	111141109
17	89649159	89649160	G	C	16	GENIC	homozygous	111141111
17	89660285	89660286	T	C	56	GENIC	homozygous	111141113
17	89661266	89661267	G	A	11	GENIC	homozygous	111141115
17	89661602	89661603	T	C	9	GENIC	homozygous	111141117
17	89662531	89662532	G	C	40	GENIC	homozygous	111141119
17	89664487	89664488	G	T	19	GENIC	homozygous	111141121
17	89664521	89664522	A	G	21	GENIC	homozygous	111141123
17	89664897	89664898	T	C	49	GENIC	homozygous	111141125
17	89665635	89665636	C	G	20	GENIC	homozygous	111141127