chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	84591245	84591246	A	G	26	GENIC	homozygous	49842687
13	84592060	84592061	T	C	23	GENIC	possibly homozygous	49842690
13	84592456	84592457	A	T	42	GENIC	homozygous	51218510
13	84592877	84592878	G	A	24	GENIC	homozygous	51218512
13	84592905	84592906	T	C	19	GENIC	possibly homozygous	51218514
13	84596788	84596792	CCTT	----	6	GENIC	homozygous	50553275
13	84596835	84596836	C	G	12	GENIC	homozygous	50440549
13	84597542	84597543	G	A	29	GENIC	possibly homozygous	51218516
13	84597895	84597896	G	A	18	GENIC	homozygous	49842716
13	84599123	84599124	G	GA	16	GENIC	heterozygous	49842726
13	84599123	84599124	G	GAAAAGAAAAAAA	16	GENIC	heterozygous	50602726
13	84600081	84600082	G	-	24	GENIC	homozygous	50566229
13	84601649	84601650	T	C	27	GENIC	homozygous	49842756
13	84601768	84601769	T	TTCACACACACAC	5	GENIC	heterozygous	50627913
13	84601769	84601775	ACACAC	------	5	GENIC	heterozygous	50584086
13	84602922	84602923	T	TAA	3	GENIC	homozygous	50414780
13	84603395	84603398	AAA	---	19	GENIC	heterozygous	50526981
13	84603396	84603398	AA	--	19	GENIC	possibly homozygous	50526983
13	84603695	84603696	A	G	33	GENIC	possibly homozygous	49842768
13	84604816	84604817	G	A	29	GENIC	possibly homozygous	49842773
13	84605367	84605368	G	A	31	GENIC	homozygous	51218518