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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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513000 SNVs 1 of 51300 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP004005515249 chr2: 35147 TW1 Intergenic A G
heterozygote
MACSNP004005515254 chr2: 35541 TW1 Intergenic T C
heterozygote
MACSNP004005515268 chr2: 37287 TW1 Intergenic T G
heterozygote
MACSNP004005515288 chr2: 38958 TW1 Intergenic A T
homozygote
MACSNP004005515294 chr2: 39703 TW1 Intergenic A T
heterozygote
MACSNP004005515321 chr2: 42083 TW1 Intergenic T C
heterozygote
MACSNP004005515333 chr2: 44101 TW1 Intergenic A G
heterozygote
MACSNP004005515335 chr2: 44341 TW1 Intergenic T C
heterozygote
MACSNP004005515338 chr2: 44498 TW1 Intergenic G A
heterozygote
MACSNP004005515348 chr2: 45628 TW1 Intergenic A G
homozygote

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