chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	103625137	103625138	A	AACAC	4	GENIC	homozygous	50534434
13	103625235	103625236	C	-	14	GENIC	homozygous	49872853
13	103629600	103629601	T	TG	39	GENIC	homozygous	49872857
13	103629601	103629602	A	C	39	GENIC	homozygous	50498713
13	103631080	103631082	TG	--	14	GENIC	heterozygous	50534436
13	103631413	103631415	GT	--	16	GENIC	heterozygous	50534438
13	103638295	103638335	GGGGACAGGGTGCTGGCCCCGGGGACAGGGTGCTGGCCCC	----------------------------------------	20	GENIC	heterozygous	50534440
13	103641882	103641884	GT	--	5	GENIC	heterozygous	50534442
13	103647118	103647119	T	TTCTG	15	GENIC	possibly homozygous	49872906
13	103655114	103655115	G	GT	11	GENIC	heterozygous	50534443
13	103655115	103655116	T	-	11	GENIC	heterozygous	50534445
13	103657040	103657041	C	CTCTGAG	23	GENIC	homozygous	49872921
13	103664654	103664655	C	CGTGT	8	GENIC	heterozygous	50534447
13	103664655	103664657	GT	--	8	GENIC	heterozygous	50150511
13	103672718	103672720	AG	--	11	GENIC	heterozygous	50534449
13	103672771	103672773	TG	--	25	GENIC	heterozygous	50534451
13	103681192	103681193	A	ATCTTCTTCT	1	GENIC	homozygous	50534453
13	103681284	103681285	C	CT	18	GENIC	homozygous	49872962
13	103683730	103683764	GAAGGAGGGAAGGGGAGGGAAGGAGGGAGGGAGG	----------------------------------	6	GENIC	homozygous	50534455
13	103690077	103690079	TC	--	12	GENIC	heterozygous	50534457
13	103691188	103691189	A	-	19	GENIC	heterozygous	50267742
13	103701519	103701520	G	GT	7	GENIC	heterozygous	50150515
13	103701520	103701521	T	-	7	GENIC	heterozygous	50534459
13	103704861	103704863	GT	--	10	GENIC	heterozygous	50534461
13	103714167	103714168	A	AG	36	GENIC	homozygous	49872989