chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	47111668	47111669	A	-	12	GENIC	possibly homozygous	52620172
8	47114106	47114107	A	-	14	GENIC	heterozygous	53550434
8	47117463	47117464	C	CT	20	GENIC	heterozygous	53109080
8	47118849	47118850	A	-	9	GENIC	heterozygous	53506718
8	47128358	47128359	G	GAA	10	GENIC	heterozygous	52620178
8	47128358	47128359	G	GAAAAAAAAAAGAA	10	GENIC	heterozygous	53381231
8	47142640	47142641	A	AAAAACAACAACCAAGGAG	6	GENIC	homozygous	53363435
8	47142641	47142642	T	TTGGGGATTTAGCTCAGTGGCAGAGCACTTGCCTAGCAAGCGCAAGGCCCTGGGTCTGGTCCCCAGCTCCGG	6	GENIC	homozygous	53363436
8	47143542	47143546	GTGT	----	9	GENIC	heterozygous	53381250
8	47157386	47157387	C	CTTT	7	GENIC	heterozygous	53381272
8	47157483	47157484	T	-	19	GENIC	homozygous	52620190
8	47157486	47157487	G	A	19	GENIC	homozygous	53381274
8	47157490	47157491	G	A	20	GENIC	homozygous	52620192
8	47157491	47157492	G	GAT	20	GENIC	homozygous	52620194
8	47162758	47162759	A	AGGTCTGGGTATACACACACACAAAACCTTGCAGCTCAGTTTTTAATTTTTGTAACATATGAATAATAGGTATATTTTAAGTCCCTGACTGACAACTTCTGTATCCTCTGTTTCTATACTCAGT	17	GENIC	homozygous	53363437
8	47167688	47167689	C	CA	18	GENIC	possibly homozygous	52620196
8	47172843	47172844	G	GTA	2	GENIC	homozygous	53618075
8	47143544	47143546	GT	--	9	GENIC	heterozygous	53429387
8	47157386	47157387	C	CT	7	GENIC	heterozygous	53429389