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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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621055 SNVs 1 of 62106 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011031370928 chr7: 25697 CE5 Intergenic G A
heterozygote
MACSNP011031370930 chr7: 25705 CE5 Intergenic T G
homozygote
MACSNP011031370935 chr7: 25766 CE5 Intergenic C G
heterozygote
MACSNP011031370936 chr7: 25961 CE5 Intergenic G A
homozygote
MACSNP011031370939 chr7: 26343 CE5 Intergenic A G
homozygote
MACSNP011031370953 chr7: 27728 CE5 Intergenic T G
heterozygote
MACSNP011031370955 chr7: 27770 CE5 Intergenic G A
homozygote
MACSNP011031370963 chr7: 28309 CE5 Intergenic C G
homozygote
MACSNP011031370970 chr7: 28641 CE5 Intergenic G A
heterozygote
MACSNP011031370980 chr7: 29042 CE5 Intergenic A T
homozygote

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