chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	82355452	82355453	G	A	56	GENIC	homozygous	114410730
13	82355548	82355549	A	G	39	GENIC	homozygous	114410732
13	82355578	82355579	C	T	47	GENIC	homozygous	114410734
13	82355656	82355657	A	G	59	GENIC	homozygous	114410736
13	82355817	82355818	C	G	59	GENIC	homozygous	114410738
13	82355922	82355923	G	C	49	GENIC	homozygous	114410740
13	82356463	82356464	A	G	53	GENIC	homozygous	114410742
13	82356986	82356987	T	C	46	GENIC	homozygous	114410744
13	82357018	82357019	A	T	41	GENIC	homozygous	114410746
13	82357047	82357048	C	T	44	GENIC	homozygous	114410748
13	82357956	82357957	C	T	64	GENIC	possibly homozygous	114410750
13	82357964	82357965	G	A	71	GENIC	possibly homozygous	114410752
13	82358087	82358088	T	C	62	GENIC	homozygous	114410754
13	82358775	82358776	T	C	61	GENIC	homozygous	114410756
13	82358959	82358960	A	G	56	GENIC	homozygous	114410758
13	82359053	82359054	C	T	58	GENIC	homozygous	114410760
13	82360684	82360684		TG	16	GENIC	homozygous	129079158
13	82357256	82357257	G		65	GENIC	homozygous	129079155
13	82357471	82357471		C	67	GENIC	homozygous	129079156
13	82358258	82358273	TGTTTGGCTCTCCCA		35	GENIC	homozygous	129079157
13	82361079	82361080	C	T	43	GENIC	homozygous	114410762
13	82361392	82361393	A	G	50	GENIC	homozygous	114410764