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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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499004 SNVs 1 of 49901 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007040365686 chr9: 202 CE1 Intergenic C T
homozygote
MACSNP007040365703 chr9: 2893 CE1 Intergenic A G
homozygote
MACSNP007040365706 chr9: 3205 CE1 Intergenic A G
homozygote
MACSNP007040365712 chr9: 3325 CE1 Intergenic T C
homozygote
MACSNP007040365713 chr9: 3379 CE1 Intergenic G T
homozygote
MACSNP007040365718 chr9: 3984 CE1 Intergenic A G
homozygote
MACSNP007040365719 chr9: 4053 CE1 Intergenic T G
homozygote
MACSNP007040365724 chr9: 4298 CE1 Intergenic T G
homozygote
MACSNP007040365727 chr9: 4322 CE1 Intergenic C T
homozygote
MACSNP007040365745 chr9: 8353 CE1 Intergenic C T
heterozygote

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