chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47648746	47648747	A		37	GENIC	possibly homozygous	132711060
13	47649095	47649096	C	A	30	GENIC	homozygous	132718999
13	47649097	47649097		AT	30	GENIC	homozygous	132711061
13	47649099	47649100	C		31	GENIC	homozygous	132711062
13	47649198	47649199	G	A	49	GENIC	homozygous	114668759
13	47649201	47649202	G	A	48	GENIC	homozygous	114668761
13	47649308	47649309	C	T	43	GENIC	homozygous	114668763
13	47649533	47649534	T	G	42	GENIC	homozygous	114668765
13	47649602	47649603	C	T	48	GENIC	homozygous	114668767
13	47649794	47649795	C	T	41	GENIC	homozygous	114668769
13	47649899	47649900	T	C	38	GENIC	homozygous	114668771
13	47649951	47649952	A		31	GENIC	homozygous	129050850
13	47649958	47649959	A		33	GENIC	homozygous	129050851
13	47649977	47649977		A	39	GENIC	homozygous	129050852
13	47649984	47649984		G	40	GENIC	homozygous	129050853
13	47649988	47649988		T	42	GENIC	homozygous	129050854
13	47650005	47650005		T	42	GENIC	homozygous	129050855
13	47650042	47650043	A		47	GENIC	homozygous	129050856
13	47650107	47650108	A	C	52	GENIC	homozygous	114548331
13	47650115	47650115		G	48	GENIC	homozygous	129050857
13	47651201	47651202	C	T	40	GENIC	homozygous	114668773
13	47650861	47650862	T	C	32	GENIC	homozygous	114760304
13	47651054	47651055	C	T	43	GENIC	homozygous	115024846