chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62305835	62305836	G	A	30	GENIC	homozygous	53274067
8	62305984	62305985	A	G	33	GENIC	homozygous	53274068
8	62306875	62306876	G	A	27	GENIC	homozygous	53274069
8	62306894	62306895	G	T	30	GENIC	homozygous	52990676
8	62307341	62307342	T	C	22	GENIC	homozygous	53274070
8	62307440	62307442	TT	--	22	GENIC	homozygous	53274071
8	62307628	62307629	C	-	18	GENIC	homozygous	52990677
8	62308164	62308165	A	-	32	GENIC	homozygous	53274072
8	62308365	62308366	T	C	38	GENIC	homozygous	53274073
8	62308784	62308785	T	G	28	GENIC	homozygous	53274074
8	62309434	62309435	A	G	34	GENIC	homozygous	53274075
8	62309614	62309615	A	G	35	GENIC	homozygous	53274076
8	62310644	62310645	A	ATTT	19	GENIC	possibly homozygous	53274077
8	62310644	62310645	A	ATT	19	GENIC	heterozygous	53274078
8	62310858	62310859	C	G	27	GENIC	possibly homozygous	53274079
8	62310859	62310860	C	CA	12	GENIC	heterozygous	52668884
8	62310859	62310860	C	CAA	12	GENIC	heterozygous	52990678
8	62311564	62311565	A	G	38	GENIC	homozygous	53274080
8	62314260	62314261	T	C	37	GENIC	homozygous	52990679
8	62314386	62314387	T	G	40	GENIC	homozygous	52990680
8	62314619	62314620	A	-	13	GENIC	heterozygous	52990681
8	62314800	62314801	A	G	55	GENIC	possibly homozygous	52990682
8	62315995	62315996	T	G	42	GENIC	homozygous	52990685
8	62316390	62316391	A	G	24	GENIC	homozygous	52990686
8	62316584	62316585	A	T	35	GENIC	homozygous	53274081
8	62316774	62316775	T	A	38	GENIC	homozygous	52990687
8	62316911	62316912	G	A	38	GENIC	homozygous	52990688
8	62317469	62317470	C	T	14	GENIC	homozygous	53274082
8	62318618	62318619	C	T	35	GENIC	homozygous	53274083
8	62315418	62315419	C	CA	17	GENIC	heterozygous	53208210