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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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671876 SNVs 1 of 67188 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP009015522748 chr4: 16801 CE3 Intergenic C T
homozygote
MACSNP009015522749 chr4: 16816 CE3 Intergenic C T
heterozygote
MACSNP009015522755 chr4: 16990 CE3 Intergenic G A
heterozygote
MACSNP009015522776 chr4: 17944 CE3 Intergenic A T
heterozygote
MACSNP009015522785 chr4: 18174 CE3 Intergenic T C
heterozygote
MACSNP009015522793 chr4: 18481 CE3 Intergenic A G
homozygote
MACSNP009015522794 chr4: 18489 CE3 Intergenic T C
heterozygote
MACSNP009015522795 chr4: 18529 CE3 Intergenic T C
heterozygote
MACSNP009015522801 chr4: 18812 CE3 Intergenic A G
heterozygote
MACSNP009015522802 chr4: 18821 CE3 Intergenic G A
heterozygote

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