chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47649951	47649952	A		40	GENIC	homozygous	129050850
13	47649958	47649959	A		41	GENIC	homozygous	129050851
13	47649977	47649977		A	41	GENIC	homozygous	129050852
13	47649984	47649984		G	45	GENIC	homozygous	129050853
13	47649988	47649988		T	45	GENIC	homozygous	129050854
13	47650005	47650005		T	45	GENIC	homozygous	129050855
13	47650042	47650043	A		54	GENIC	homozygous	129050856
13	47650107	47650108	A	C	49	GENIC	homozygous	114548331
13	47650115	47650115		G	48	GENIC	homozygous	129050857
13	47650195	47650195		T	13	GENIC	homozygous	131919391
13	47650197	47650197		A	11	GENIC	homozygous	131919392
13	47650201	47650202	T		11	GENIC	homozygous	131919393
13	47650207	47650207		T	9	GENIC	homozygous	131919394
13	47650213	47650213		C	9	GENIC	homozygous	131919395
13	47650218	47650219	A	C	7	GENIC	homozygous	131925046
13	47650239	47650240	T	C	5	GENIC	homozygous	131925047
13	47650258	47650259	T		2	GENIC	homozygous	131919396
13	47650262	47650262		C	2	GENIC	homozygous	131919397
13	47650271	47650272	T		9	GENIC	homozygous	131919398