chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11659457	11659458	C	T	13	GENIC	homozygous	47020594
17	11659579	11659580	T	C	17	GENIC	homozygous	47020595
17	11660190	11660191	G	A	15	GENIC	heterozygous	47914215
17	11660570	11660571	A	G	16	GENIC	homozygous	47020596
17	11661499	11661500	T	G	13	GENIC	homozygous	47020608
17	11662428	11662429	G	T	10	GENIC	heterozygous	47020610
17	11662508	11662509	T	A	10	GENIC	heterozygous	47020611
17	11663530	11663531	T	TC	13	GENIC	homozygous	47020613
17	11663661	11663662	A	G	9	GENIC	heterozygous	47020614
17	11663748	11663749	C	A	12	GENIC	heterozygous	47914216
17	11663978	11663979	C	T	15	GENIC	homozygous	47020615
17	11664823	11664824	G	A	25	GENIC	heterozygous	47020616
17	11664862	11664863	C	A	21	GENIC	heterozygous	47020617
17	11664927	11664931	CCCA	----	17	GENIC	heterozygous	47914217
17	11665380	11665381	G	A	11	GENIC	homozygous	47020621
17	11665633	11665634	T	C	13	GENIC	heterozygous	47914219
17	11666001	11666002	T	C	9	GENIC	homozygous	47020622
17	11664920	11664921	C	-	17	GENIC	heterozygous	47284674