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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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512418 SNVs 1 of 51242 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010046690003 chr11: 76 CE4 Intergenic A G
homozygote
MACSNP010046690007 chr11: 168 CE4 Intergenic T C
homozygote
MACSNP010046690019 chr11: 562 CE4 Intergenic G A
homozygote
MACSNP010046690024 chr11: 694 CE4 Intergenic C T
homozygote
MACSNP010046690029 chr11: 805 CE4 Intergenic C T
homozygote
MACSNP010046690031 chr11: 835 CE4 Intergenic T C
homozygote
MACSNP010046690033 chr11: 945 CE4 Intergenic C T
homozygote
MACSNP010046690035 chr11: 974 CE4 Intergenic G A
homozygote
MACSNP010046690042 chr11: 1220 CE4 Intergenic C T
homozygote
MACSNP010046690048 chr11: 1386 CE4 Intergenic G C
homozygote

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