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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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702750 SNVs 1 of 70275 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007005515239 chr2: 34364 CE1 Intergenic C T
heterozygote
MACSNP007005515246 chr2: 34761 CE1 Intergenic A G
heterozygote
MACSNP007005515247 chr2: 34879 CE1 Intergenic A T
heterozygote
MACSNP007005515258 chr2: 35762 CE1 Intergenic A T
homozygote
MACSNP007005515264 chr2: 36967 CE1 Intergenic C T
heterozygote
MACSNP007005515270 chr2: 37608 CE1 Intergenic T C
homozygote
MACSNP007005515275 chr2: 37977 CE1 Intergenic T A
heterozygote
MACSNP007005515279 chr2: 38356 CE1 Intergenic C A
heterozygote
MACSNP007005515288 chr2: 38958 CE1 Intergenic A T
heterozygote
MACSNP007005515289 chr2: 39246 CE1 Intergenic A C
heterozygote

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