chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	95665930	95665946	GTTGGTTTGTTGGTTT	----------------	41	GENIC	heterozygous	50531396
13	95670211	95670212	T	TCTCA	40	GENIC	heterozygous	50531398
13	95670278	95670279	C	CTT	55	GENIC	heterozygous	50497688
13	95670305	95670306	A	ATCTGCTACACCGCAAGTGG	60	GENIC	heterozygous	50497689
13	95675771	95675775	ATAT	----	6	GENIC	heterozygous	50531400
13	95675812	95675816	TATA	----	1	GENIC	homozygous	50531402
13	95678503	95678505	GG	--	190	GENIC	possibly homozygous	50497690
13	95678504	95678505	G	GCTTA	186	GENIC	possibly homozygous	50497691
13	95678507	95678509	TG	--	197	GENIC	possibly homozygous	50531404
13	95678520	95678522	AA	--	215	GENIC	possibly homozygous	50497692
13	95678521	95678522	A	AGGC	210	GENIC	possibly homozygous	50497693
13	95678775	95678776	A	-	209	GENIC	heterozygous	49861064
13	95678911	95678913	GG	--	152	GENIC	heterozygous	50531406
13	95679376	95679377	G	GT	159	GENIC	heterozygous	49861076
13	95679434	95679442	TGAGAGAA	--------	37	GENIC	heterozygous	50531408
13	95679569	95679570	G	GGGT	237	GENIC	heterozygous	49861081
13	95679602	95679603	A	AGGCTTCCCTGACCG	223	GENIC	possibly homozygous	49861083
13	95679772	95679773	G	GCC	152	GENIC	heterozygous	50531410
13	95679836	95679837	T	TCTTGGC	57	GENIC	heterozygous	50531412
13	95679849	95679850	C	CCTGGCG	41	GENIC	heterozygous	50531414
13	95679992	95679993	T	TAC	33	GENIC	heterozygous	49861095
13	95680021	95680022	T	G	32	GENIC	heterozygous	49861096
13	95681095	95681096	G	GTA	23	GENIC	heterozygous	50531416
13	95681209	95681216	CGCCGGT	-------	11	GENIC	heterozygous	49861113
13	95681502	95681503	C	CACCA	84	GENIC	heterozygous	49861117
13	95682056	95682060	TCCA	----	10	GENIC	homozygous	50531418