chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	63091346	63091347	A	-	16	GENIC	possibly homozygous	52992284
8	63091923	63091924	A	G	34	GENIC	homozygous	52992286
8	63092978	63092979	G	A	25	GENIC	homozygous	53320857
8	63094177	63094188	TCCTGCCAACG	-----------	12	GENIC	homozygous	53320858
8	63095000	63095001	A	G	29	GENIC	homozygous	52992290
8	63095638	63095639	T	-	24	GENIC	homozygous	53208227
8	63095670	63095671	T	TG	19	GENIC	possibly homozygous	53320859
8	63095322	63095328	TGTGTG	------	3	GENIC	homozygous	53389688
8	63097471	63097473	AC	--	6	GENIC	homozygous	53389690
8	63098851	63098853	TG	--	18	GENIC	homozygous	53320860
8	63099354	63099355	A	G	16	GENIC	homozygous	52992297
8	63099671	63099672	G	GT	16	GENIC	homozygous	53320861
8	63100841	63100842	T	A	29	GENIC	homozygous	53320862
8	63101506	63101507	C	T	25	GENIC	homozygous	53320863
8	63109847	63109848	C	G	17	GENIC	homozygous	53320864
8	63109912	63109913	G	GT	12	GENIC	homozygous	53320865
8	63112096	63112097	T	A	23	GENIC	homozygous	52992324
8	63112346	63112347	G	A	30	GENIC	homozygous	53320866
8	63112867	63112868	A	AG	17	GENIC	heterozygous	53320867
8	63113244	63113245	T	C	35	GENIC	homozygous	53320868
8	63113314	63113315	G	A	31	GENIC	homozygous	53320869
8	63113660	63113661	C	T	33	GENIC	possibly homozygous	53320870
8	63113880	63113881	A	AGTGGATGGACAG	29	GENIC	homozygous	53320871
8	63114802	63114803	T	C	27	GENIC	homozygous	52992332
8	63114841	63114842	A	G	26	GENIC	homozygous	52992333
8	63115033	63115037	CACA	----	7	GENIC	homozygous	53389692
8	63115374	63115375	C	T	24	GENIC	homozygous	53320872
8	63115851	63115852	T	TTGTGTG	11	GENIC	heterozygous	53389693
8	63115851	63115852	T	TTGTGTGTG	11	GENIC	heterozygous	53389694
8	63108124	63108125	C	CA	17	GENIC	homozygous	52669247
8	63109346	63109348	AC	--	29	GENIC	heterozygous	52669249