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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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651559 SNVs 1 of 65156 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP008031370799 chr7: 2907 CE2 Intergenic T C
heterozygote
MACSNP008031370800 chr7: 2921 CE2 Intergenic G A
heterozygote
MACSNP008031370801 chr7: 2959 CE2 Intergenic T C
heterozygote
MACSNP008031370802 chr7: 2972 CE2 Intergenic G T
heterozygote
MACSNP008031370803 chr7: 3180 CE2 Intergenic G A
heterozygote
MACSNP008031370804 chr7: 3522 CE2 Intergenic G A
heterozygote
MACSNP008031370805 chr7: 3554 CE2 Intergenic C A
heterozygote
MACSNP008031370806 chr7: 3718 CE2 Intergenic C T
heterozygote
MACSNP008031370807 chr7: 3727 CE2 Intergenic T C
heterozygote
MACSNP008031370808 chr7: 4171 CE2 Intergenic T G
heterozygote

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