chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	100982073	100982075	GT	--	23	GENIC	heterozygous	50533819
13	100982821	100982822	A	ATCTCTC	2	GENIC	homozygous	50603341
13	100983173	100983177	TCTC	----	11	GENIC	heterozygous	50533821
13	100987209	100987210	C	CA	20	GENIC	heterozygous	50533823
13	100987210	100987211	A	-	20	GENIC	heterozygous	50533825
13	100987533	100987534	A	AAAG	13	GENIC	heterozygous	50533827
13	100989800	100989801	A	-	4	GENIC	heterozygous	50533829
13	101003976	101003977	A	T	1	GENIC	homozygous	49867453
13	101003981	101003982	G	T	1	GENIC	homozygous	49867454
13	101003982	101003983	G	T	1	GENIC	homozygous	49867455
13	101003983	101003984	G	A	1	GENIC	homozygous	50533833
13	101003985	101003986	G	A	1	GENIC	homozygous	49974000
13	101003988	101003989	G	C	2	GENIC	homozygous	49867456
13	101004075	101004076	G	-	10	GENIC	homozygous	49867457
13	101004339	101004340	G	-	38	GENIC	homozygous	49867458
13	101004346	101004347	G	-	40	GENIC	homozygous	49867459
13	101004356	101004357	G	-	35	GENIC	homozygous	49867460
13	101004371	101004373	GT	--	36	GENIC	homozygous	49867462
13	101004381	101004382	G	-	39	GENIC	homozygous	49867463
13	101004426	101004427	G	-	32	GENIC	homozygous	49867464
13	101004430	101004431	G	-	32	GENIC	homozygous	49867465
13	101004433	101004434	G	-	33	GENIC	homozygous	49867466
13	101004447	101004448	G	-	33	GENIC	homozygous	49867467
13	101004450	101004453	TGG	---	36	GENIC	homozygous	49867468
13	101005119	101005120	C	CT	3	GENIC	heterozygous	50533835