chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39713559	39713560	C	T	27	GENIC	homozygous	52963120
8	39715112	39715113	G	A	32	GENIC	homozygous	52963121
8	39716304	39716305	G	-	21	GENIC	heterozygous	52591496
8	39716324	39716325	T	-	26	GENIC	heterozygous	52591497
8	39716329	39716330	G	-	26	GENIC	heterozygous	52591498
8	39717295	39717296	C	T	27	GENIC	homozygous	52963122
8	39717621	39717622	T	C	37	GENIC	homozygous	52591500
8	39720958	39720959	A	G	36	GENIC	homozygous	52591510
8	39722254	39722255	A	AAC	33	GENIC	heterozygous	52963123
8	39722257	39722259	AC	--	33	GENIC	heterozygous	53101695
8	39723462	39723463	G	A	24	GENIC	homozygous	52963124
8	39727968	39727969	T	G	43	GENIC	heterozygous	52963126
8	39729468	39729469	A	G	20	GENIC	homozygous	52591523
8	39729513	39729514	C	CG	21	GENIC	homozygous	52591524
8	39730036	39730037	G	-	20	GENIC	homozygous	52591529
8	39733051	39733052	C	G	22	GENIC	heterozygous	52963127
8	39733053	39733054	A	C	17	GENIC	possibly homozygous	52591539
8	39733093	39733094	A	AT	11	GENIC	heterozygous	52591540
8	39733094	39733095	A	T	15	GENIC	homozygous	52591541
8	39734880	39734881	G	GC	15	GENIC	homozygous	52591547
8	39734905	39734906	G	GAA	16	GENIC	homozygous	52591548
8	39734910	39734911	C	A	17	GENIC	homozygous	52591549