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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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159780 SNVs 1 of 15978 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP009070912480 chr19: 27963 CE3 Intergenic C T
heterozygote
MACSNP009070912482 chr19: 28071 CE3 Intergenic A G
heterozygote
MACSNP009070912485 chr19: 28135 CE3 Intergenic G A
heterozygote
MACSNP009070912486 chr19: 28149 CE3 Intergenic G A
heterozygote
MACSNP009070912490 chr19: 28218 CE3 Intergenic T A
heterozygote
MACSNP009070912491 chr19: 28230 CE3 Intergenic T G
heterozygote
MACSNP009070912493 chr19: 28271 CE3 Intergenic A T
heterozygote
MACSNP009070912494 chr19: 28285 CE3 Intergenic G C
heterozygote
MACSNP009070912495 chr19: 28317 CE3 Intergenic G A
heterozygote
MACSNP009070912496 chr19: 28345 CE3 Intergenic T C
heterozygote

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