chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	17145123	17145124	A	G	26	GENIC	homozygous	48547698
14	17145234	17145235	C	T	30	GENIC	possibly homozygous	48547699
14	17145237	17145238	C	T	30	GENIC	possibly homozygous	48547700
14	17145436	17145437	A	T	27	GENIC	possibly homozygous	48547701
14	17146881	17146882	T	C	23	GENIC	homozygous	48547703
14	17147292	17147293	T	A	28	GENIC	homozygous	48547704
14	17147594	17147595	T	C	17	GENIC	homozygous	48547705
14	17148593	17148594	A	-	4	GENIC	homozygous	48956520
14	17146431	17146432	G	GTTT	9	GENIC	homozygous	48956514
14	17146645	17146649	AATC	----	13	GENIC	homozygous	48956516
14	17147961	17147963	TA	--	8	GENIC	homozygous	48956518
14	17149038	17149039	C	T	26	GENIC	homozygous	48956524
14	17149298	17149299	T	C	29	GENIC	homozygous	48547713
14	17149753	17149754	A	G	18	GENIC	homozygous	48956526
14	17149761	17149762	A	G	17	GENIC	homozygous	48956528
14	17149763	17149764	T	G	17	GENIC	homozygous	48956530
14	17149811	17149812	A	T	29	GENIC	homozygous	48956532
14	17149861	17149862	A	G	31	GENIC	homozygous	48956534
14	17149905	17149906	C	A	27	GENIC	homozygous	48956536
14	17149971	17149972	A	G	28	GENIC	possibly homozygous	48956538
14	17150080	17150081	G	A	15	GENIC	homozygous	48956540
14	17150192	17150193	A	G	20	GENIC	homozygous	48956542