chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	17145123	17145124	A	G	63	GENIC	homozygous	48547698
14	17145234	17145235	C	T	40	GENIC	homozygous	48547699
14	17145237	17145238	C	T	40	GENIC	homozygous	48547700
14	17145436	17145437	A	T	60	GENIC	homozygous	48547701
14	17146431	17146432	G	GTT	24	GENIC	possibly homozygous	48547702
14	17146431	17146432	G	GTTT	24	GENIC	heterozygous	48956514
14	17146881	17146882	T	C	33	GENIC	possibly homozygous	48547703
14	17147292	17147293	T	A	37	GENIC	homozygous	48547704
14	17147594	17147595	T	C	41	GENIC	homozygous	48547705
14	17147751	17147752	T	G	38	GENIC	homozygous	48547706
14	17147945	17147947	TG	--	4	GENIC	heterozygous	48547707
14	17147961	17147963	TA	--	1	GENIC	homozygous	48956518
14	17148603	17148604	A	AG	20	GENIC	heterozygous	48547708
14	17148603	17148604	A	AAG	20	GENIC	possibly homozygous	48547709
14	17148935	17148936	C	T	40	GENIC	possibly homozygous	48547710
14	17148978	17148979	T	G	46	GENIC	homozygous	48547711
14	17149078	17149079	G	A	38	GENIC	homozygous	48547712
14	17149298	17149299	T	C	51	GENIC	homozygous	48547713
14	17149307	17149308	C	T	49	GENIC	homozygous	48547714
14	17150175	17150176	G	A	28	GENIC	homozygous	48547715