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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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369166 SNVs 1 of 36917 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011043964663 chr10: 460 CE5 Intergenic G A
homozygote
MACSNP011043964702 chr10: 1147 CE5 Intergenic A G
heterozygote
MACSNP011043964704 chr10: 1230 CE5 Intergenic T C
heterozygote
MACSNP011043964716 chr10: 2836 CE5 Intergenic T A
heterozygote
MACSNP011043964717 chr10: 3233 CE5 Intergenic G A
heterozygote
MACSNP011043964719 chr10: 3416 CE5 Intergenic C A
heterozygote
MACSNP011043964720 chr10: 3527 CE5 Intergenic C T
heterozygote
MACSNP011043964724 chr10: 3691 CE5 Intergenic T C
heterozygote
MACSNP011043964727 chr10: 3752 CE5 Intergenic T C
heterozygote
MACSNP011043964742 chr10: 4256 CE5 Intergenic A G
heterozygote

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