chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	2066618	2066619	A	G	23	GENIC	homozygous	48447578
14	2068116	2068117	C	T	32	GENIC	homozygous	48936647
14	2068530	2068531	C	T	36	GENIC	homozygous	48936648
14	2069480	2069481	A	G	30	GENIC	homozygous	48936649
14	2069628	2069629	T	C	27	GENIC	homozygous	48447581
14	2070887	2070888	A	G	31	GENIC	homozygous	48447583
14	2071323	2071324	A	G	32	GENIC	homozygous	48936650
14	2071994	2071995	C	T	28	GENIC	homozygous	48936651
14	2072818	2072819	G	C	30	GENIC	homozygous	48936652
14	2073029	2073030	C	CT	35	GENIC	homozygous	48447588
14	2073447	2073448	G	GA	32	GENIC	homozygous	48936653
14	2073448	2073449	C	T	32	GENIC	homozygous	49270813
14	2073812	2073813	G	A	22	GENIC	homozygous	48447590
14	2074136	2074137	A	G	25	GENIC	homozygous	48447591
14	2074210	2074211	C	T	26	GENIC	homozygous	48447592
14	2074390	2074391	C	T	29	GENIC	homozygous	48936654
14	2074398	2074399	A	G	26	GENIC	homozygous	48936655
14	2074837	2074838	C	T	36	GENIC	homozygous	48936656
14	2075022	2075023	C	T	31	GENIC	homozygous	48936657
14	2075266	2075267	G	A	19	GENIC	homozygous	48936658
14	2076057	2076058	G	A	14	GENIC	homozygous	48936659
14	2077067	2077068	G	A	20	GENIC	homozygous	48936660
14	2078633	2078634	A	G	27	GENIC	homozygous	48447597
14	2078845	2078846	A	-	30	GENIC	homozygous	48447599