chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	85686733	85686734	T	C	21	GENIC	homozygous	142408835
13	85688374	85688375	T	C	19	GENIC	homozygous	142408836
13	85688429	85688430	G	T	17	GENIC	homozygous	142408837
13	85688469	85688469		GGTCCCGAA	18	GENIC	homozygous	142352225
13	85688516	85688517	C	A	13	GENIC	homozygous	142408838
13	85688625	85688626	A	G	25	GENIC	homozygous	142408839
13	85688830	85688830		A	17	GENIC	homozygous	142352226
13	85688858	85688859	A	C	19	GENIC	homozygous	142408840
13	85689037	85689038	C	A	20	GENIC	homozygous	142408841
13	85689374	85689377	AAG		4	GENIC	heterozygous	142352227
13	85689994	85689995	T	C	24	GENIC	homozygous	142408842
13	85691004	85691005	G	T	23	GENIC	homozygous	142408843
13	85691154	85691155	A	C	20	GENIC	homozygous	142408844
13	85691405	85691406	A	C	14	GENIC	homozygous	142408845
13	85691787	85691788	A	G	18	GENIC	homozygous	142408846