chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62000924	62000925	T	-	27	GENIC	homozygous	52668722
8	62002696	62002697	A	-	2	GENIC	homozygous	53182200
8	62006700	62006701	G	C	25	GENIC	homozygous	52668724
8	62006705	62006706	G	-	27	GENIC	homozygous	52668726
8	62006783	62006784	A	G	17	GENIC	homozygous	52668732
8	62006791	62006792	T	C	18	GENIC	homozygous	52668734
8	62006795	62006796	T	C	18	GENIC	homozygous	52668736
8	62006803	62006804	G	C	18	GENIC	homozygous	52668738
8	62006806	62006807	G	GTGCTT	19	GENIC	homozygous	52668740
8	62007456	62007457	C	CA	8	GENIC	heterozygous	52668743
8	62012709	62012710	A	-	16	GENIC	heterozygous	52989723
8	62012962	62012963	C	T	30	GENIC	heterozygous	52668747
8	62013007	62013008	A	G	49	GENIC	heterozygous	52668749
8	62013008	62013009	T	TG	43	GENIC	heterozygous	52668751
8	62013046	62013047	T	C	57	GENIC	heterozygous	52668753
8	62016430	62016431	A	ATT	14	GENIC	homozygous	52668755
8	62017212	62017213	C	CA	6	GENIC	homozygous	52668757
8	62017218	62017219	A	AG	10	GENIC	homozygous	52668759
8	62017286	62017287	G	T	14	GENIC	homozygous	52668761
8	62017604	62017622	TCTCTTCTCTCTCTCTCT	------------------	13	GENIC	heterozygous	52668763
8	62017608	62017609	T	-	14	GENIC	homozygous	52668765
8	62017608	62017609	T	TC	14	GENIC	homozygous	52668767
8	62017621	62017622	T	-	13	GENIC	possibly homozygous	52668769
8	62017621	62017622	T	TC	13	GENIC	homozygous	52668771
8	62017780	62017781	C	CAT	15	GENIC	homozygous	52668773
8	62017782	62017783	G	-	13	GENIC	homozygous	52668775
8	62017785	62017786	A	-	16	GENIC	homozygous	52668777
8	62020113	62020114	T	-	5	GENIC	heterozygous	52668779
8	62024174	62024175	C	CGT	17	GENIC	heterozygous	52668781