chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	43680583	43680584	T	C	37	GENIC	homozygous	111053499
17	43680897	43680898	A	G	33	GENIC	homozygous	111053501
17	43680999	43681000	C	T	26	GENIC	possibly homozygous	111053503
17	43681261	43681262	G	A	39	GENIC	homozygous	111053506
17	43681262	43681263	A	T	39	GENIC	homozygous	111053508
17	43681648	43681649	G	A	34	GENIC	homozygous	111053510
17	43681649	43681650	C	A	34	GENIC	homozygous	111053512
17	43681656	43681657	G	A	33	GENIC	homozygous	111053514
17	43682451	43682452	C	G	25	GENIC	homozygous	111053516
17	43683383	43683384	T	C	24	GENIC	homozygous	111053518
17	43683980	43683981	C	A	34	GENIC	homozygous	111053520
17	43684368	43684369	T	C	32	GENIC	homozygous	111053522
17	43684386	43684387	C	A	27	GENIC	homozygous	111053524
17	43685427	43685428	T	C	11	GENIC	homozygous	119286370
17	43686692	43686693	T	C	38	GENIC	homozygous	111053526
17	43686736	43686737	T	C	38	GENIC	homozygous	111053528
17	43686847	43686848	A	G	29	GENIC	homozygous	111053530
17	43686935	43686936	T	C	34	GENIC	homozygous	111053532
17	43687771	43687772	G	T	39	GENIC	homozygous	111053534
17	43687817	43687818	A	C	39	GENIC	homozygous	111053536
17	43688668	43688668		TTGTACCAATACGTAA	32	GENIC	homozygous	129451367
17	43687441	43687454	CTCTCACAGGCAA		16	GENIC	homozygous	129451363
17	43687622	43687625	TTG		23	GENIC	homozygous	129451364
17	43688013	43688013		A	39	GENIC	homozygous	129451365
17	43688625	43688625		AT	38	GENIC	homozygous	129451366
17	43687468	43687504	ACACACACACACACACACACACACACACGGGGGGGG		21	GENIC	heterozygous	132215575
17	43688737	43688738	C	A	43	GENIC	possibly homozygous	111053538
17	43688749	43688750	G	A	42	GENIC	homozygous	111053540
17	43688934	43688935	T	C	26	GENIC	homozygous	119286372
17	43689012	43689013	G	A	29	GENIC	homozygous	119286373
17	43689225	43689226	G	C	31	GENIC	homozygous	111053542
17	43689231	43689232	A	T	31	GENIC	homozygous	111053544