chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	61999392	61999394	AT	--	7	GENIC	heterozygous	53124677
8	62002696	62002697	A	-	11	GENIC	heterozygous	53182200
8	62006795	62006796	T	C	15	GENIC	homozygous	52668736
8	62000924	62000925	T	-	13	GENIC	homozygous	52668722
8	62006700	62006701	G	C	21	GENIC	homozygous	52668724
8	62006705	62006706	G	-	20	GENIC	homozygous	52668726
8	62006768	62006769	G	A	15	GENIC	possibly homozygous	52668728
8	62006771	62006772	A	G	13	GENIC	homozygous	52668730
8	62006783	62006784	A	G	11	GENIC	homozygous	52668732
8	62006791	62006792	T	C	13	GENIC	homozygous	52668734
8	62006803	62006804	G	C	15	GENIC	homozygous	52668738
8	62006806	62006807	G	GTGCTT	15	GENIC	homozygous	52668740
8	62013008	62013009	T	TG	43	GENIC	heterozygous	52668751
8	62013396	62013397	C	CGT	4	GENIC	heterozygous	53509589
8	62013397	62013399	GT	--	4	GENIC	heterozygous	53509591
8	62016430	62016431	A	ATT	13	GENIC	homozygous	52668755
8	62016433	62016434	G	A	13	GENIC	homozygous	53389305
8	62016436	62016437	G	T	12	GENIC	homozygous	53389306
8	62016438	62016439	G	T	9	GENIC	homozygous	53389307
8	62017212	62017213	C	CA	8	GENIC	homozygous	52668757
8	62017218	62017219	A	AG	7	GENIC	homozygous	52668759
8	62017286	62017287	G	T	15	GENIC	homozygous	52668761
8	62017608	62017609	T	-	4	GENIC	heterozygous	52668765
8	62017621	62017622	T	-	4	GENIC	homozygous	52668769
8	62017781	62017783	CG	--	20	GENIC	homozygous	53389308
8	62017783	62017784	A	AT	19	GENIC	homozygous	53389309
8	62017785	62017786	A	AC	21	GENIC	homozygous	53389310
8	62020113	62020114	T	-	12	GENIC	possibly homozygous	52668779
8	62024174	62024175	C	CGT	6	GENIC	homozygous	52668781