chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11659457	11659458	C	T	55	GENIC	possibly homozygous	47020594
17	11659579	11659580	T	C	46	GENIC	homozygous	47020595
17	11660570	11660571	A	G	42	GENIC	possibly homozygous	47020596
17	11660813	11660814	T	C	23	GENIC	homozygous	47020597
17	11660850	11660866	TTTTTTTTTTTTTTCC	----------------	7	GENIC	heterozygous	47020598
17	11660864	11660866	CC	--	14	GENIC	homozygous	47020599
17	11661073	11661074	C	CT	3	GENIC	homozygous	47020600
17	11661299	11661300	C	T	42	GENIC	heterozygous	47020601
17	11661302	11661303	C	T	41	GENIC	heterozygous	47020602
17	11661324	11661325	A	G	45	GENIC	possibly homozygous	47020603
17	11661327	11661328	A	G	46	GENIC	possibly homozygous	47020604
17	11661363	11661364	G	A	44	GENIC	heterozygous	47020605
17	11661372	11661373	G	A	42	GENIC	heterozygous	47020606
17	11661384	11661385	A	G	41	GENIC	heterozygous	47365591
17	11661400	11661401	G	A	46	GENIC	heterozygous	47020607
17	11661499	11661500	T	G	40	GENIC	homozygous	47020608
17	11662290	11662291	G	A	46	GENIC	homozygous	47020609
17	11662428	11662429	G	T	49	GENIC	homozygous	47020610
17	11662508	11662509	T	A	45	GENIC	homozygous	47020611
17	11662913	11662914	A	-	36	GENIC	homozygous	47020612
17	11663530	11663531	T	TC	49	GENIC	homozygous	47020613
17	11663661	11663662	A	G	34	GENIC	homozygous	47020614
17	11663978	11663979	C	T	50	GENIC	possibly homozygous	47020615
17	11664823	11664824	G	A	33	GENIC	homozygous	47020616
17	11664862	11664863	C	A	35	GENIC	homozygous	47020617
17	11665364	11665365	G	GAAAA	27	GENIC	homozygous	47020618
17	11665375	11665376	G	A	43	GENIC	heterozygous	47020620
17	11665380	11665381	G	A	41	GENIC	possibly homozygous	47020621
17	11666001	11666002	T	C	28	GENIC	possibly homozygous	47020622