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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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452005 SNVs 1 of 45201 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP012053619584 chr13: 1834 TM1 Intergenic G T
homozygote
MACSNP012053619621 chr13: 9684 TM1 Intergenic C G
homozygote
MACSNP012053619678 chr13: 16555 TM1 Intergenic G C
heterozygote
MACSNP012053619679 chr13: 16571 TM1 Intergenic G A
heterozygote
MACSNP012053619680 chr13: 16578 TM1 Intergenic A G
homozygote
MACSNP012053619698 chr13: 18826 TM1 Intergenic C A
homozygote
MACSNP012053619711 chr13: 19946 TM1 Intergenic C T
homozygote
MACSNP012053619714 chr13: 19993 TM1 Intergenic A G
homozygote
MACSNP012053619721 chr13: 20194 TM1 Intergenic T G
heterozygote
MACSNP012053619731 chr13: 20625 TM1 Intergenic T C
heterozygote

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