chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	61999988	61999989	T	C	19	GENIC	homozygous	53300500
8	62000155	62000156	A	AAATAATAAT	12	GENIC	possibly homozygous	53929872
8	62004429	62004445	GTGTGTGTGTGTGTGT	----------------	11	GENIC	heterozygous	53433689
8	62005688	62005689	T	TTCTCTCTCTC	5	GENIC	heterozygous	53550805
8	62006768	62006769	G	A	19	GENIC	homozygous	52668728
8	62000924	62000925	T	-	21	GENIC	homozygous	52668722
8	62006700	62006701	G	C	36	GENIC	homozygous	52668724
8	62006705	62006706	G	-	34	GENIC	homozygous	52668726
8	62005688	62005689	T	TTCTCTCTC	5	GENIC	heterozygous	53389294
8	62006771	62006772	A	G	19	GENIC	homozygous	52668730
8	62006783	62006784	A	G	21	GENIC	homozygous	52668732
8	62006791	62006792	T	C	22	GENIC	homozygous	52668734
8	62006795	62006796	T	C	22	GENIC	homozygous	52668736
8	62006803	62006804	G	C	23	GENIC	homozygous	52668738
8	62006806	62006807	G	GTGCTT	23	GENIC	homozygous	52668740
8	62011896	62011900	AGAT	----	5	GENIC	homozygous	53633643
8	62013008	62013009	T	TG	47	GENIC	heterozygous	52668751
8	62013396	62013397	C	CGT	3	GENIC	heterozygous	53509589
8	62013396	62013397	C	CGTGTGTGT	3	GENIC	heterozygous	53618521
8	62013531	62013532	G	GGT	16	GENIC	heterozygous	53576298
8	62016430	62016431	A	ATT	12	GENIC	homozygous	52668755
8	62016433	62016434	G	A	12	GENIC	homozygous	53389305
8	62016436	62016437	G	T	12	GENIC	homozygous	53389306
8	62016438	62016439	G	T	12	GENIC	homozygous	53389307
8	62017212	62017213	C	CG	9	GENIC	heterozygous	53273557
8	62017286	62017287	G	T	22	GENIC	homozygous	52668761
8	62017212	62017213	C	CA	9	GENIC	possibly homozygous	52668757
8	62017218	62017219	A	AG	9	GENIC	homozygous	52668759
8	62017621	62017622	T	-	4	GENIC	heterozygous	52668769
8	62017781	62017783	CG	--	18	GENIC	homozygous	53389308
8	62017783	62017784	A	AT	18	GENIC	homozygous	53389309
8	62017785	62017786	A	AC	18	GENIC	homozygous	53389310
8	62020113	62020114	T	-	5	GENIC	homozygous	52668779