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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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701853 SNVs 1 of 70186 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP008015522695 chr4: 947 CE2 Intergenic G C
homozygote
MACSNP008015522696 chr4: 958 CE2 Intergenic G C
heterozygote
MACSNP008015522697 chr4: 1088 CE2 Intergenic C T
heterozygote
MACSNP008015522698 chr4: 3561 CE2 Intergenic T C
homozygote
MACSNP008015522699 chr4: 4181 CE2 Intergenic T G
heterozygote
MACSNP008015522700 chr4: 4781 CE2 Intergenic T C
heterozygote
MACSNP008015522701 chr4: 4914 CE2 Intergenic T C
heterozygote
MACSNP008015522702 chr4: 4924 CE2 Intergenic T C
heterozygote
MACSNP008015522703 chr4: 4974 CE2 Intergenic T C
homozygote
MACSNP008015522704 chr4: 5601 CE2 Intergenic A G
heterozygote

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