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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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861133 SNVs 1 of 86114 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP018026079066 chr6: 17623 PM2 Intergenic C T
homozygote
MACSNP018026079088 chr6: 24613 PM2 Intergenic C T
homozygote
MACSNP018026079089 chr6: 24679 PM2 Intergenic G A
homozygote
MACSNP018026079098 chr6: 26263 PM2 Intergenic G A
heterozygote
MACSNP018026079099 chr6: 26827 PM2 Intergenic A G
heterozygote
MACSNP018026079100 chr6: 26867 PM2 Intergenic G C
homozygote
MACSNP018026079107 chr6: 28178 PM2 Intergenic C T
homozygote
MACSNP018026079117 chr6: 30507 PM2 Intergenic G A
homozygote
MACSNP018026079123 chr6: 38486 PM2 Intergenic T C
heterozygote
MACSNP018026079125 chr6: 38548 PM2 Intergenic C T
heterozygote

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