chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	49420888	49420889	G	A	29	GENIC	homozygous	116488279
8	49422674	49422675	T	G	23	GENIC	homozygous	116488281
8	49422766	49422767	G	A	8	GENIC	homozygous	116488283
8	49423324	49423325	C	T	26	GENIC	homozygous	116488285
8	49423402	49423403	C	T	34	GENIC	homozygous	116488287
8	49423403	49423404	A	G	34	GENIC	homozygous	116488289
8	49423805	49423806	G	A	23	GENIC	homozygous	116488291
8	49423907	49423908	C	T	19	GENIC	homozygous	116488293
8	49424198	49424199	G	A	31	GENIC	homozygous	116488295
8	49424244	49424245	C	A	27	GENIC	homozygous	116488297
8	49424363	49424364	T	G	27	GENIC	homozygous	116488299
8	49424384	49424385	C	T	28	GENIC	homozygous	116488301
8	49424425	49424426	A	T	33	GENIC	homozygous	116488303
8	49424475	49424476	G	A	34	GENIC	homozygous	116488305
8	49425682	49425683	G	A	19	GENIC	homozygous	116488307
8	49427526	49427527	T	C	32	GENIC	homozygous	116488311
8	49427623	49427624	C	A	33	GENIC	homozygous	116488313
8	49427969	49427970	G	T	40	GENIC	homozygous	116488315
8	49427970	49427971	A	T	40	GENIC	homozygous	116488317
8	49428093	49428094	C	T	31	GENIC	homozygous	116488319
8	49428696	49428697	T	C	25	GENIC	homozygous	116488321
8	49430422	49430423	G	A	28	GENIC	homozygous	116488325