chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	103625137	103625138	A	AACAC	1	GENIC	homozygous	50534434
13	103625235	103625236	C	-	55	GENIC	homozygous	49872853
13	103629600	103629601	T	TG	53	GENIC	homozygous	49872857
13	103631080	103631082	TG	--	20	GENIC	heterozygous	50534436
13	103631413	103631415	GT	--	3	GENIC	heterozygous	50534438
13	103638295	103638335	GGGGACAGGGTGCTGGCCCCGGGGACAGGGTGCTGGCCCC	----------------------------------------	32	GENIC	heterozygous	50534440
13	103641882	103641884	GT	--	10	GENIC	heterozygous	50534442
13	103647118	103647119	T	TTCTG	17	GENIC	homozygous	49872906
13	103655115	103655116	T	-	7	GENIC	heterozygous	50534445
13	103657040	103657041	C	CTCTGAG	43	GENIC	homozygous	49872921
13	103681192	103681193	A	ATCTTCTTCT	1	GENIC	homozygous	50534453
13	103681284	103681285	C	CT	7	GENIC	homozygous	49872962
13	103683419	103683423	ACAC	----	20	GENIC	heterozygous	50586881
13	103683421	103683423	AC	--	20	GENIC	heterozygous	50586882
13	103683730	103683764	GAAGGAGGGAAGGGGAGGGAAGGAGGGAGGGAGG	----------------------------------	6	GENIC	homozygous	50534455
13	103691188	103691189	A	-	6	GENIC	heterozygous	50267742
13	103629601	103629602	A	C	54	GENIC	homozygous	50498713
13	103697758	103697759	C	CTGTGTGTGTG	18	GENIC	heterozygous	50554139
13	103697759	103697761	TG	--	18	GENIC	heterozygous	50554141
13	103714167	103714168	A	AG	29	GENIC	homozygous	49872989