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Filter SNVs Using Feature Selection

Chromosome chr1 chr2 chr3 chr4 chr5 chr6 chr7 chr8 chr9 chr10 chr11 chr12 chr13 chr14 chr15 chr16 chr17 chr18 chr19 chr20
Individual All CR1 CR2 CR3 TW1 JM1 JM2 CE1 CE2 CE3 CE4 CE5 TM1 TM2 AM1 SM1 SM2 PM1 PM2 LM1 BM1
Gene feature All CDS EXON 3'UTR INTRON 5'UTR Genotype All homozygote heterozygote Mutation All non-synonymous synonymous
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344135 SNVs 1 of 34414 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006056871527 chr14: 3761 JM2 Intergenic T C
homozygote
MACSNP006056871545 chr14: 4551 JM2 Intergenic C T
homozygote
MACSNP006056871551 chr14: 4684 JM2 Intergenic A T
homozygote
MACSNP006056871578 chr14: 5582 JM2 Intergenic C T
homozygote
MACSNP006056871579 chr14: 5615 JM2 Intergenic A G
heterozygote
MACSNP006056871588 chr14: 5882 JM2 Intergenic C T
homozygote
MACSNP006056871604 chr14: 6463 JM2 Intergenic T C
homozygote
MACSNP006056871610 chr14: 6664 JM2 Intergenic T C
homozygote
MACSNP006056871615 chr14: 6775 JM2 Intergenic A G
heterozygote
MACSNP006056871616 chr14: 6799 JM2 Intergenic C T
heterozygote

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