chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	103625235	103625236	C	-	18	GENIC	homozygous	49872853
13	103629600	103629601	T	TG	25	GENIC	homozygous	49872857
13	103629601	103629602	A	C	24	GENIC	homozygous	50498713
13	103631413	103631415	GT	--	8	GENIC	heterozygous	50534438
13	103638295	103638335	GGGGACAGGGTGCTGGCCCCGGGGACAGGGTGCTGGCCCC	----------------------------------------	24	GENIC	heterozygous	50534440
13	103641882	103641884	GT	--	7	GENIC	heterozygous	50534442
13	103647118	103647119	T	TTCTG	4	GENIC	homozygous	49872906
13	103655114	103655115	G	GT	8	GENIC	heterozygous	50534443
13	103655115	103655116	T	-	8	GENIC	heterozygous	50534445
13	103657040	103657041	C	CTCTGAG	30	GENIC	homozygous	49872921
13	103664655	103664657	GT	--	6	GENIC	heterozygous	50150511
13	103668508	103668509	T	-	22	GENIC	heterozygous	49872953
13	103672771	103672773	TG	--	22	GENIC	heterozygous	50534451
13	103681284	103681285	C	CT	11	GENIC	homozygous	49872962
13	103683730	103683764	GAAGGAGGGAAGGGGAGGGAAGGAGGGAGGGAGG	----------------------------------	5	GENIC	homozygous	50534455
13	103690077	103690079	TC	--	10	GENIC	heterozygous	50534457
13	103697759	103697761	TG	--	8	GENIC	heterozygous	50554141
13	103704861	103704863	GT	--	4	GENIC	heterozygous	50534461
13	103705723	103705724	A	AGTGT	1	GENIC	homozygous	50613343
13	103714167	103714168	A	AG	30	GENIC	homozygous	49872989