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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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728645 SNVs 1 of 72865 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP008005515245 chr2: 34635 CE2 Intergenic A G
heterozygote
MACSNP008005515250 chr2: 35282 CE2 Intergenic T G
heterozygote
MACSNP008005515258 chr2: 35762 CE2 Intergenic A T
heterozygote
MACSNP008005515260 chr2: 36495 CE2 Intergenic G A
heterozygote
MACSNP008005515268 chr2: 37287 CE2 Intergenic T G
heterozygote
MACSNP008005515270 chr2: 37608 CE2 Intergenic T C
heterozygote
MACSNP008005515272 chr2: 37707 CE2 Intergenic A G
heterozygote
MACSNP008005515279 chr2: 38356 CE2 Intergenic C A
heterozygote
MACSNP008005515288 chr2: 38958 CE2 Intergenic A T
heterozygote
MACSNP008005515291 chr2: 39585 CE2 Intergenic A G
heterozygote

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