chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	65676384	65676385	A	C	37	GENIC	homozygous	47166404
17	65676522	65676523	C	G	32	GENIC	heterozygous	47166405
17	65678657	65678659	GG	--	14	GENIC	heterozygous	47166406
17	65678658	65678659	G	-	14	GENIC	heterozygous	47166407
17	65678671	65678672	A	G	17	GENIC	heterozygous	47166408
17	65678886	65678910	AGCCCAATAGCCCAATAGCCCAAT	------------------------	5	GENIC	homozygous	47166409
17	65686115	65686116	C	CAG	5	GENIC	homozygous	47166411
17	65678747	65678748	C	CTTT	11	GENIC	homozygous	47546604
17	65680280	65680282	GT	--	12	GENIC	homozygous	47546606
17	65685697	65685698	T	C	48	GENIC	homozygous	47546608
17	65688517	65688518	A	G	46	GENIC	homozygous	47166412
17	65690860	65690864	TTTT	----	13	GENIC	homozygous	47166413
17	65690872	65690873	T	TC	20	GENIC	heterozygous	47337347
17	65690882	65690883	C	CT	15	GENIC	heterozygous	47337349
17	65691583	65691584	C	G	25	GENIC	possibly homozygous	47546610
17	65691688	65691689	A	T	27	GENIC	possibly homozygous	47166414
17	65691872	65691886	TGTGTGTGTGTGTG	--------------	13	GENIC	possibly homozygous	47166415
17	65694805	65694806	G	C	35	GENIC	heterozygous	47546612
17	65694807	65694808	C	CTG	31	GENIC	heterozygous	47166420
17	65694809	65694810	C	G	35	GENIC	heterozygous	47166421
17	65695274	65695275	A	G	39	GENIC	homozygous	47166422
17	65695547	65695548	A	AACAC	3	GENIC	homozygous	47166424