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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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730533 SNVs 1 of 73054 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP009000000008 chr1: 9562 CE3 Intergenic C T
heterozygote
MACSNP009000000011 chr1: 9620 CE3 Intergenic C T
homozygote
MACSNP009000000015 chr1: 9719 CE3 Intergenic C T
heterozygote
MACSNP009000000021 chr1: 9800 CE3 Intergenic G C
homozygote
MACSNP009000000045 chr1: 10390 CE3 Intergenic T C
homozygote
MACSNP009000000053 chr1: 10506 CE3 Intergenic C T
heterozygote
MACSNP009000000054 chr1: 10515 CE3 Intergenic G A
homozygote
MACSNP009000000062 chr1: 10652 CE3 Intergenic G A
homozygote
MACSNP009000000066 chr1: 10787 CE3 Intergenic G A
heterozygote
MACSNP009000000068 chr1: 10823 CE3 Intergenic G A
heterozygote

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