chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47452479	47452480	C	T	31	GENIC	homozygous	114614714
13	47453778	47453779	G	A	38	GENIC	possibly homozygous	114614715
13	47453840	47453841	C	A	45	GENIC	homozygous	114614716
13	47454907	47454908	G	A	51	GENIC	homozygous	114614717
13	47454988	47454989	C	A	43	GENIC	homozygous	114614718
13	47455962	47455963	T	G	63	GENIC	homozygous	114614719
13	47456146	47456147	A	T	54	GENIC	homozygous	114614720
13	47456330	47456331	A	G	41	GENIC	homozygous	114614721
13	47456739	47456740	T	G	52	GENIC	homozygous	114614722
13	47456740	47456741	T	A	53	GENIC	homozygous	114614723
13	47457766	47457767	G	C	58	GENIC	homozygous	114614724
13	47459158	47459159	A	G	64	GENIC	heterozygous	118497215
13	47459764	47459765	T	C	48	GENIC	homozygous	114614725
13	47462193	47462194	G	A	31	GENIC	homozygous	114614726
13	47462265	47462266	G	A	36	GENIC	heterozygous	118566782
13	47462269	47462270	A	G	36	GENIC	heterozygous	118535335
13	47464191	47464192	A	G	56	GENIC	homozygous	114614727
13	47464517	47464518	G	T	50	GENIC	homozygous	114614728
13	47464652	47464653	C	T	52	GENIC	possibly homozygous	114614729
13	47464703	47464704	C	T	57	GENIC	homozygous	114614730
13	47464734	47464735	G	A	72	GENIC	homozygous	114614731
13	47464760	47464761	C	T	77	GENIC	homozygous	114614732
13	47464998	47464999	C	T	32	GENIC	homozygous	114719989
13	47466434	47466435	G	C	45	GENIC	possibly homozygous	114614733