chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	53647784	53647785	C	T	10	GENIC	homozygous	53363856
8	53648469	53648470	C	-	29	GENIC	homozygous	52634240
8	53648476	53648477	C	A	35	GENIC	possibly homozygous	53363857
8	53649377	53649379	AA	--	11	GENIC	heterozygous	53363858
8	53649378	53649379	A	-	11	GENIC	heterozygous	53363859
8	53649770	53649771	A	G	37	GENIC	homozygous	52634244
8	53649921	53649929	TGAATGAA	--------	32	GENIC	homozygous	52634246
8	53650301	53650302	C	G	24	GENIC	homozygous	52634248
8	53650461	53650462	A	G	25	GENIC	homozygous	52634250
8	53650505	53650506	T	-	13	GENIC	heterozygous	53387307
8	53653637	53653638	T	-	23	GENIC	homozygous	52634252
8	53653762	53653763	G	A	24	GENIC	homozygous	52634256
8	53653772	53653773	A	G	23	GENIC	homozygous	52634258
8	53653794	53653795	G	A	27	GENIC	homozygous	52634260
8	53654172	53654173	T	-	6	GENIC	heterozygous	52634265
8	53654296	53654297	C	CTGTGTGTG	7	GENIC	homozygous	53431274
8	53654668	53654669	G	A	25	GENIC	homozygous	52634267
8	53654723	53654724	T	G	31	GENIC	homozygous	52634269
8	53654768	53654769	T	C	32	GENIC	homozygous	52634271
8	53653807	53653808	T	C	26	GENIC	homozygous	52976430
8	53654627	53654628	C	-	25	GENIC	homozygous	52976431