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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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635383 SNVs 1 of 63539 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011010706154 chr3: 6077 CE5 Intergenic A C
homozygote
MACSNP011010706180 chr3: 7292 CE5 Intergenic C G
homozygote
MACSNP011010706182 chr3: 7519 CE5 Intergenic T C
homozygote
MACSNP011010706185 chr3: 7904 CE5 Intergenic C A
heterozygote
MACSNP011010706209 chr3: 9708 CE5 Intergenic T C
heterozygote
MACSNP011010706233 chr3: 11551 CE5 Intergenic C T
homozygote
MACSNP011010706234 chr3: 11575 CE5 Intergenic T C
homozygote
MACSNP011010706240 chr3: 11867 CE5 Intergenic G C
homozygote
MACSNP011010706249 chr3: 12218 CE5 Intergenic A G
homozygote
MACSNP011010706261 chr3: 12576 CE5 Intergenic A C
heterozygote

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