chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	89115306	89115307	C	T	23	GENIC	homozygous	116972885
8	89116389	89116390	G	A	21	GENIC	homozygous	116972886
8	89117960	89117961	T	C	29	GENIC	homozygous	116559411
8	89119885	89119886	C	T	20	GENIC	homozygous	116972887
8	89120302	89120303	C	T	34	GENIC	homozygous	116972888
8	89120620	89120621	C	G	37	GENIC	possibly homozygous	116972889
8	89120630	89120631	G	A	40	GENIC	heterozygous	116972890
8	89121313	89121314	G	A	38	GENIC	homozygous	116972891
8	89121865	89121866	G	C	25	GENIC	homozygous	116972892
8	89123171	89123172	T	C	19	GENIC	homozygous	116972893
8	89123739	89123740	A	G	21	GENIC	homozygous	116559439
8	89123910	89123911	T	C	24	GENIC	homozygous	116559441
8	89124079	89124080	C	T	29	GENIC	homozygous	116972894
8	89124229	89124230	G	A	22	GENIC	homozygous	116972895
8	89127024	89127025	G	A	41	GENIC	homozygous	116972896
8	89129426	89129427	G	A	15	GENIC	homozygous	116972897