chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	95407726	95407727	T	C	11	GENIC	homozygous	50141384
13	95409919	95409929	GTGTGTGTGT	----------	6	GENIC	heterozygous	50585190
13	95409927	95409929	GT	--	6	GENIC	heterozygous	50531342
13	95411277	95411278	T	A	39	GENIC	homozygous	50141392
13	95413027	95413030	GGT	---	12	GENIC	homozygous	50141398
13	95413977	95413978	T	TAAAA	18	GENIC	heterozygous	50141402
13	95413977	95413978	T	TAAA	18	GENIC	possibly homozygous	50367511
13	95410586	95410587	G	A	15	GENIC	homozygous	51141215
13	95411075	95411076	G	C	37	GENIC	possibly homozygous	51141216
13	95411352	95411355	GTG	---	22	GENIC	homozygous	51141217
13	95411970	95411971	G	A	21	GENIC	homozygous	51141218
13	95408598	95408599	C	G	14	GENIC	possibly homozygous	51037360