chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	47555551	47555552	C	CCTGGAACTAGAGTTGTAGGCAGCTAGTTGTGAGCTGCCTGTTCCCTGGAAGAGATCAGAAGAGAGTGTCCGGTCTGGGGTTAGAGATAGATGCAGATTCTGAAAACTGAACCTGGGTCTTCTGCCTGAAGAAT	16	GENIC	homozygous	53381750
8	47555604	47555605	C	-	5	GENIC	homozygous	53429441
8	47558607	47558608	A	ATTATTTAT	5	GENIC	heterozygous	54145246
8	47560470	47560471	T	-	7	GENIC	heterozygous	52620333
8	47569559	47569563	TTTA	----	2	GENIC	homozygous	53429445
8	47572432	47572433	C	CT	10	GENIC	heterozygous	53506751
8	47572433	47572434	T	-	10	GENIC	heterozygous	53381772
8	47574495	47574496	G	GA	10	GENIC	possibly homozygous	53381774
8	47576153	47576154	T	TA	10	GENIC	homozygous	52620345
8	47576484	47576485	T	-	7	GENIC	heterozygous	53460170
8	47576487	47576491	TTTT	----	9	GENIC	heterozygous	53460171
8	47577258	47577259	T	-	21	GENIC	possibly homozygous	52620347
8	47577357	47577358	A	AAAC	20	GENIC	heterozygous	53646361
8	47578113	47578115	TC	--	32	GENIC	heterozygous	53603889
8	47578295	47578296	A	AG	33	GENIC	heterozygous	52620379
8	47579409	47579410	A	AT	34	GENIC	heterozygous	52620387