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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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652099 SNVs 1 of 65210 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010010706154 chr3: 6077 CE4 Intergenic A C
homozygote
MACSNP010010706156 chr3: 6158 CE4 Intergenic T C
homozygote
MACSNP010010706161 chr3: 6498 CE4 Intergenic A G
homozygote
MACSNP010010706180 chr3: 7292 CE4 Intergenic C G
homozygote
MACSNP010010706182 chr3: 7519 CE4 Intergenic T C
homozygote
MACSNP010010706200 chr3: 8872 CE4 Intergenic G C
heterozygote
MACSNP010010706209 chr3: 9708 CE4 Intergenic T C
homozygote
MACSNP010010706210 chr3: 9738 CE4 Intergenic G A
heterozygote
MACSNP010010706233 chr3: 11551 CE4 Intergenic C T
homozygote
MACSNP010010706234 chr3: 11575 CE4 Intergenic T C
homozygote

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