chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	103625235	103625236	C	-	19	GENIC	homozygous	49872853
13	103629600	103629601	T	TG	24	GENIC	homozygous	49872857
13	103631080	103631082	TG	--	13	GENIC	heterozygous	50534436
13	103638295	103638335	GGGGACAGGGTGCTGGCCCCGGGGACAGGGTGCTGGCCCC	----------------------------------------	20	GENIC	heterozygous	50534440
13	103641882	103641884	GT	--	6	GENIC	heterozygous	50534442
13	103647118	103647119	T	TTCTG	15	GENIC	possibly homozygous	49872906
13	103657040	103657041	C	CTCTGAG	19	GENIC	homozygous	49872921
13	103681192	103681193	A	ATCTTCTTCT	1	GENIC	homozygous	50534453
13	103629601	103629602	A	C	24	GENIC	homozygous	50498713
13	103631405	103631415	GTGTGTGTGT	----------	16	GENIC	homozygous	50554136
13	103672662	103672664	CA	--	5	GENIC	heterozygous	50566616
13	103681284	103681285	C	CT	17	GENIC	homozygous	49872962
13	103683730	103683764	GAAGGAGGGAAGGGGAGGGAAGGAGGGAGGGAGG	----------------------------------	4	GENIC	homozygous	50534455
13	103688547	103688548	C	-	15	GENIC	heterozygous	49872969
13	103690076	103690077	T	TTC	10	GENIC	possibly homozygous	50554138
13	103697758	103697759	C	CTG	12	GENIC	heterozygous	50566617
13	103697758	103697759	C	CTGTGTGTGTG	12	GENIC	heterozygous	50554139
13	103697759	103697761	TG	--	12	GENIC	heterozygous	50554141
13	103701519	103701520	G	GT	5	GENIC	heterozygous	50150515
13	103701520	103701521	T	-	5	GENIC	heterozygous	50534459
13	103704861	103704863	GT	--	4	GENIC	heterozygous	50534461
13	103714167	103714168	A	AG	29	GENIC	homozygous	49872989