chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	47245760	47245761	T	C	30	GENIC	homozygous	53962430
8	47247280	47247281	T	A	29	GENIC	possibly homozygous	53962432
8	47247651	47247652	G	A	29	GENIC	homozygous	53181619
8	47249499	47249503	TCTG	----	22	GENIC	homozygous	53962434
8	47249863	47249864	G	A	30	GENIC	homozygous	53962436
8	47249933	47249934	T	C	35	GENIC	homozygous	53181620
8	47250451	47250452	T	C	16	GENIC	possibly homozygous	53962438
8	47250684	47250685	G	A	33	GENIC	possibly homozygous	53109272
8	47250777	47250778	C	T	29	GENIC	homozygous	53181622
8	47251457	47251458	C	A	22	GENIC	homozygous	53109273
8	47252099	47252101	AA	--	8	GENIC	homozygous	53109274
8	47252149	47252150	C	CAAAAAAAAAAAAAA	10	GENIC	homozygous	53363438
8	47252265	47252266	A	G	20	GENIC	homozygous	53109275
8	47252270	47252271	A	T	19	GENIC	homozygous	53962440
8	47252326	47252335	AGGGGAAGG	---------	7	GENIC	possibly homozygous	53962442
8	47252349	47252352	GAA	---	10	GENIC	heterozygous	53962444
8	47252366	47252367	G	-	11	GENIC	heterozygous	53962446
8	47252386	47252388	AT	--	20	GENIC	homozygous	53962449
8	47252619	47252620	T	C	29	GENIC	homozygous	53109278
8	47252769	47252770	A	G	32	GENIC	homozygous	53109279
8	47253517	47253518	T	A	30	GENIC	homozygous	53962451
8	47253591	47253592	T	C	27	GENIC	homozygous	53109280
8	47253727	47253730	TCC	---	27	GENIC	homozygous	53181623
8	47254130	47254131	C	G	21	GENIC	homozygous	53181624
8	47254386	47254387	G	A	22	GENIC	possibly homozygous	53962453
8	47254540	47254541	C	T	14	GENIC	homozygous	53962455
8	47254544	47254547	AAA	---	11	GENIC	heterozygous	53109282
8	47254950	47254951	C	CACG	24	GENIC	homozygous	53962457