chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	84572115	84572116	T	C	59	GENIC	possibly homozygous	51722969
10	84572649	84572650	T	G	82	GENIC	homozygous	51722971
10	84573524	84573525	G	-	13	GENIC	heterozygous	51523651
10	84573529	84573533	GTCT	----	11	GENIC	possibly homozygous	51523653
10	84573921	84573922	T	C	69	GENIC	homozygous	51722973
10	84574111	84574112	C	T	56	GENIC	homozygous	51722975
10	84574356	84574357	T	C	63	GENIC	homozygous	51523656
10	84574389	84574390	T	C	62	GENIC	homozygous	51722977
10	84574788	84574789	A	C	53	GENIC	homozygous	51722980
10	84574852	84574853	T	C	64	GENIC	homozygous	51722982
10	84574927	84574928	T	C	60	GENIC	homozygous	51722984
10	84575199	84575200	T	C	79	GENIC	homozygous	51722986
10	84575680	84575681	G	A	63	GENIC	homozygous	51722988
10	84576162	84576163	A	C	57	GENIC	homozygous	51722990
10	84576985	84576986	G	C	50	GENIC	homozygous	51523658
10	84576986	84576987	G	C	48	GENIC	homozygous	51523659
10	84576987	84576988	G	C	48	GENIC	possibly homozygous	51523661
10	84577187	84577188	C	T	56	GENIC	homozygous	51722992
10	84577548	84577549	A	G	52	GENIC	homozygous	51722994
10	84577728	84577729	T	C	61	GENIC	homozygous	51722996
10	84578081	84578082	A	-	27	GENIC	homozygous	51722998
10	84578109	84578135	CCTGGAGGTTCAACAAGGGAATGTCT	--------------------------	23	GENIC	homozygous	51722999
10	84578111	84578112	T	C	17	GENIC	homozygous	51723001
10	84578247	84578248	C	T	46	GENIC	homozygous	51723003
10	84578477	84578478	G	T	50	GENIC	heterozygous	51723005
10	84578480	84578481	G	A	53	GENIC	possibly homozygous	51723007
10	84578858	84578859	G	T	43	GENIC	possibly homozygous	51723009
10	84580129	84580130	A	T	53	GENIC	homozygous	51723011
10	84580201	84580202	G	A	63	GENIC	homozygous	51723013