chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	103625235	103625236	C	-	13	GENIC	homozygous	49872853
13	103629600	103629601	T	TG	34	GENIC	homozygous	49872857
13	103629601	103629602	A	C	36	GENIC	homozygous	50498713
13	103631413	103631415	GT	--	6	GENIC	heterozygous	50534438
13	103638295	103638335	GGGGACAGGGTGCTGGCCCCGGGGACAGGGTGCTGGCCCC	----------------------------------------	14	GENIC	heterozygous	50534440
13	103647118	103647119	T	TTCTG	12	GENIC	possibly homozygous	49872906
13	103655114	103655115	G	GT	8	GENIC	heterozygous	50534443
13	103655115	103655116	T	-	8	GENIC	heterozygous	50534445
13	103657040	103657041	C	CTCTGAG	36	GENIC	homozygous	49872921
13	103658580	103658581	T	TAAA	12	GENIC	heterozygous	49872928
13	103664654	103664655	C	CGTGT	3	GENIC	heterozygous	50534447
13	103664655	103664657	GT	--	3	GENIC	heterozygous	50150511
13	103681284	103681285	C	CT	15	GENIC	homozygous	49872962
13	103683730	103683764	GAAGGAGGGAAGGGGAGGGAAGGAGGGAGGGAGG	----------------------------------	2	GENIC	homozygous	50534455
13	103690076	103690077	T	TTC	3	GENIC	heterozygous	50554138
13	103697758	103697759	C	CTGTGTGTGTG	5	GENIC	heterozygous	50554139
13	103697759	103697761	TG	--	5	GENIC	heterozygous	50554141
13	103703358	103703362	CTGT	----	13	GENIC	heterozygous	50620326
13	103704861	103704863	GT	--	1	GENIC	homozygous	50534461