chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	16268095	16268097	CT		43	GENIC	homozygous	129128549
14	16268357	16268358	A	G	32	GENIC	homozygous	113357773
14	16269000	16269001	T	C	55	GENIC	homozygous	113357775
14	16269098	16269099	G	A	42	GENIC	homozygous	113357777
14	16269324	16269325	C	T	36	GENIC	homozygous	113357779
14	16269699	16269700	T	C	43	GENIC	homozygous	113357781
14	16270210	16270211	G	A	51	GENIC	homozygous	113357783
14	16270739	16270740	A	G	34	GENIC	possibly homozygous	113357785
14	16271731	16271732	C	T	33	GENIC	homozygous	113357787
14	16271883	16271884	C	T	36	GENIC	homozygous	113357789
14	16272564	16272565	C	A	48	GENIC	homozygous	113357791
14	16273580	16273581	T	C	53	GENIC	homozygous	113357793
14	16273606	16273608	AC		43	GENIC	homozygous	129128550
14	16273955	16273958	TTG		18	GENIC	heterozygous	129128551
14	16274261	16274261		AAAC	28	GENIC	possibly homozygous	129128552
14	16274915	16274916	T	C	48	GENIC	homozygous	113357797
14	16275146	16275147	A	G	57	GENIC	possibly homozygous	113357799
14	16275297	16275298	G	A	45	GENIC	homozygous	113357801
14	16275955	16275956	C	T	40	GENIC	homozygous	113357803
14	16275989	16275990	T	C	43	GENIC	homozygous	113357805
14	16273942	16273943	T	G	25	GENIC	homozygous	113908385