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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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706220 SNVs 1 of 70622 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP009026079057 chr6: 13336 CE3 Intergenic A G
heterozygote
MACSNP009026079070 chr6: 22783 CE3 Intergenic C T
homozygote
MACSNP009026079100 chr6: 26867 CE3 Intergenic G C
homozygote
MACSNP009026079130 chr6: 39077 CE3 Intergenic T C
homozygote
MACSNP009026079135 chr6: 39552 CE3 Intergenic T A
homozygote
MACSNP009026079138 chr6: 39787 CE3 Intergenic C A
homozygote
MACSNP009026079152 chr6: 43465 CE3 Intergenic T C
homozygote
MACSNP009026079156 chr6: 43911 CE3 Intergenic A G
homozygote
MACSNP009026079157 chr6: 44343 CE3 Intergenic A C
homozygote
MACSNP009026079165 chr6: 44719 CE3 Intergenic T C
homozygote

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