chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	80366502	80366503	G	T	62	GENIC	homozygous	47199349
17	80366921	80366922	A	G	55	GENIC	heterozygous	47199350
17	80366921	80366922	A	ACG	48	GENIC	heterozygous	47199351
17	80367159	80367160	C	T	42	GENIC	possibly homozygous	47199352
17	80367435	80367436	T	C	51	GENIC	homozygous	47199353
17	80367617	80367618	A	AAAAC	16	GENIC	heterozygous	47199354
17	80367781	80367782	G	A	17	GENIC	homozygous	47199355
17	80368434	80368435	G	A	29	GENIC	homozygous	47199356
17	80368672	80368673	A	G	45	GENIC	homozygous	47199357
17	80369483	80369484	A	G	45	GENIC	homozygous	47199358
17	80369574	80369575	A	C	57	GENIC	homozygous	47199359
17	80369785	80369786	A	G	35	GENIC	homozygous	47199360
17	80370560	80370561	G	A	49	GENIC	homozygous	47199361
17	80370715	80370716	T	A	49	GENIC	homozygous	47199362
17	80371195	80371196	G	A	39	GENIC	homozygous	47199363
17	80371598	80371599	T	G	37	GENIC	homozygous	47199364
17	80371685	80371687	CG	--	41	GENIC	homozygous	47199365
17	80371828	80371829	A	G	30	GENIC	homozygous	47199366
17	80371964	80371965	T	C	56	GENIC	homozygous	47199367
17	80372005	80372006	T	C	53	GENIC	homozygous	47199368
17	80372024	80372025	G	GCA	35	GENIC	homozygous	47199369
17	80373623	80373624	G	A	34	GENIC	homozygous	47199370
17	80375735	80375736	T	C	50	GENIC	homozygous	47199371
17	80376101	80376102	G	GT	19	GENIC	possibly homozygous	47199372
17	80376101	80376102	G	GTTT	19	GENIC	heterozygous	47199373
17	80376187	80376188	T	-	27	GENIC	homozygous	47199374
17	80376782	80376783	A	T	46	GENIC	possibly homozygous	47199375
17	80376783	80376784	C	A	50	GENIC	possibly homozygous	47199376