chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	105762547	105762548	G	GA	6	GENIC	heterozygous	49976662
13	105762549	105762551	AA	--	6	GENIC	heterozygous	49976663
13	105767280	105767281	T	A	6	GENIC	homozygous	49873882
13	105767282	105767283	T	C	5	GENIC	homozygous	49873883
13	105767541	105767543	GT	--	17	GENIC	heterozygous	49976668
13	105768081	105768085	TTCC	----	6	GENIC	homozygous	49873884
13	105768082	105768084	TC	--	17	GENIC	heterozygous	50202043
13	105768177	105768179	AC	--	2	GENIC	homozygous	49873885
13	105769387	105769389	CC	--	57	GENIC	heterozygous	49873887
13	105769387	105769388	C	CA	58	GENIC	heterozygous	49873888
13	105769388	105769389	C	CT	59	GENIC	heterozygous	49873889
13	105769389	105769391	CA	--	59	GENIC	heterozygous	49873890
13	105769490	105769493	TCC	---	107	GENIC	heterozygous	49873892
13	105769495	105769496	C	A	196	GENIC	heterozygous	50202045
13	105769510	105769511	A	C	175	GENIC	heterozygous	49976678
13	105769511	105769514	TCC	---	95	GENIC	heterozygous	49976679
13	105769666	105769667	A	-	48	GENIC	heterozygous	49873894
13	105788890	105788891	A	AGT	22	GENIC	heterozygous	49873897
13	105788898	105788900	TA	--	28	GENIC	heterozygous	49873898
13	105788903	105788904	A	ATG	31	GENIC	heterozygous	49873899
13	105788994	105788995	A	AGT	25	GENIC	heterozygous	49873900
13	105789021	105789022	G	A	41	GENIC	heterozygous	49873901
13	105789040	105789041	A	AGTGT	22	GENIC	possibly homozygous	49873902
13	105789051	105789052	G	GTATT	27	GENIC	heterozygous	49873904
13	105769513	105769514	C	A	169	GENIC	heterozygous	50150880