chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11659457	11659458	C	T	7	GENIC	possibly homozygous	47020594
17	11659579	11659580	T	C	6	GENIC	homozygous	47020595
17	11660570	11660571	A	G	11	GENIC	possibly homozygous	47020596
17	11660813	11660814	T	C	2	GENIC	homozygous	47020597
17	11661400	11661401	G	A	5	GENIC	heterozygous	47020607
17	11661499	11661500	T	G	13	GENIC	homozygous	47020608
17	11662290	11662291	G	A	16	GENIC	possibly homozygous	47020609
17	11662428	11662429	G	T	7	GENIC	possibly homozygous	47020610
17	11662508	11662509	T	A	7	GENIC	homozygous	47020611
17	11662913	11662914	A	-	5	GENIC	heterozygous	47020612
17	11663530	11663531	T	TC	7	GENIC	possibly homozygous	47020613
17	11663661	11663662	A	G	14	GENIC	homozygous	47020614
17	11663978	11663979	C	T	7	GENIC	heterozygous	47020615
17	11664823	11664824	G	A	11	GENIC	possibly homozygous	47020616
17	11664862	11664863	C	A	3	GENIC	homozygous	47020617
17	11665364	11665365	G	GAAAA	2	GENIC	homozygous	47020618
17	11665380	11665381	G	A	5	GENIC	homozygous	47020621
17	11666001	11666002	T	C	2	GENIC	heterozygous	47020622