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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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298299 SNVs 1 of 29830 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011068733179 chr18: 226 CE5 Intergenic C T
heterozygote
MACSNP011068733193 chr18: 569 CE5 Intergenic C G
heterozygote
MACSNP011068733194 chr18: 569 CE5 Intergenic C G
heterozygote
MACSNP011068733204 chr18: 695 CE5 Intergenic T C
heterozygote
MACSNP011068733216 chr18: 901 CE5 Intergenic T G
heterozygote
MACSNP011068733217 chr18: 931 CE5 Intergenic C T
homozygote
MACSNP011068733238 chr18: 1868 CE5 Intergenic T C
heterozygote
MACSNP011068733244 chr18: 2051 CE5 Intergenic T C
homozygote
MACSNP011068733248 chr18: 2220 CE5 Intergenic A G
homozygote
MACSNP011068733269 chr18: 2752 CE5 Intergenic T G
heterozygote

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