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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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421531 SNVs 1 of 42154 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP008065724298 chr17: 37654 CE2 Intergenic A G
homozygote
MACSNP008065724305 chr17: 37752 CE2 Intergenic G A
heterozygote
MACSNP008065724310 chr17: 37813 CE2 Intergenic T C
homozygote
MACSNP008065724313 chr17: 37841 CE2 Intergenic C T
homozygote
MACSNP008065724316 chr17: 37873 CE2 Intergenic G A
homozygote
MACSNP008065724322 chr17: 37946 CE2 Intergenic C A
heterozygote
MACSNP008065724329 chr17: 37998 CE2 Intergenic G A
heterozygote
MACSNP008065724332 chr17: 38026 CE2 Intergenic T C
homozygote
MACSNP008065724335 chr17: 38046 CE2 Intergenic G C
heterozygote
MACSNP008065724342 chr17: 38130 CE2 Intergenic A T
heterozygote

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