chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11659457	11659458	C	T	39	GENIC	homozygous	47020594
17	11659579	11659580	T	C	35	GENIC	homozygous	47020595
17	11660570	11660571	A	G	20	GENIC	homozygous	47020596
17	11660813	11660814	T	C	29	GENIC	homozygous	47020597
17	11660850	11660866	TTTTTTTTTTTTTTCC	----------------	20	GENIC	possibly homozygous	47020598
17	11661324	11661325	A	G	50	GENIC	homozygous	47020603
17	11661327	11661328	A	G	52	GENIC	homozygous	47020604
17	11661400	11661401	G	A	41	GENIC	homozygous	47020607
17	11661499	11661500	T	G	30	GENIC	homozygous	47020608
17	11662428	11662429	G	T	28	GENIC	homozygous	47020610
17	11662508	11662509	T	A	37	GENIC	homozygous	47020611
17	11663530	11663531	T	TC	29	GENIC	homozygous	47020613
17	11663661	11663662	A	G	27	GENIC	homozygous	47020614
17	11663978	11663979	C	T	30	GENIC	homozygous	47020615
17	11664823	11664824	G	A	11	GENIC	homozygous	47020616
17	11664862	11664863	C	A	16	GENIC	homozygous	47020617
17	11665364	11665365	G	GAAA	9	GENIC	homozygous	47020619
17	11665380	11665381	G	A	17	GENIC	homozygous	47020621
17	11665384	11665385	G	A	14	GENIC	homozygous	47365593
17	11666001	11666002	T	C	19	GENIC	homozygous	47020622
17	11664920	11664921	C	-	18	GENIC	homozygous	47284674