chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62305835	62305836	G	A	16	GENIC	homozygous	53274067
8	62305984	62305985	A	G	7	GENIC	homozygous	53274068
8	62306875	62306876	G	A	15	GENIC	homozygous	53274069
8	62306894	62306895	G	T	14	GENIC	homozygous	52990676
8	62307312	62307314	TG	--	6	GENIC	heterozygous	53320181
8	62307341	62307342	T	C	8	GENIC	homozygous	53274070
8	62307440	62307442	TT	--	12	GENIC	homozygous	53274071
8	62307599	62307600	A	-	14	GENIC	heterozygous	53701002
8	62308164	62308165	A	-	8	GENIC	homozygous	53274072
8	62308365	62308366	T	C	20	GENIC	homozygous	53274073
8	62308784	62308785	T	G	19	GENIC	homozygous	53274074
8	62309434	62309435	A	G	15	GENIC	homozygous	53274075
8	62309614	62309615	A	G	15	GENIC	homozygous	53274076
8	62310160	62310161	C	T	17	GENIC	heterozygous	53701003
8	62310858	62310859	C	G	8	GENIC	homozygous	53274079
8	62311564	62311565	A	G	11	GENIC	homozygous	53274080
8	62314386	62314387	T	G	11	GENIC	homozygous	52990680
8	62315995	62315996	T	G	8	GENIC	homozygous	52990685
8	62316390	62316391	A	G	20	GENIC	homozygous	52990686
8	62316774	62316775	T	A	9	GENIC	homozygous	52990687
8	62316911	62316912	G	A	18	GENIC	homozygous	52990688
8	62318746	62318747	C	T	12	GENIC	heterozygous	53320184