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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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742389 SNVs 1 of 74239 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP015015522743 chr4: 16388 SM1 Intergenic G A
homozygote
MACSNP015015522747 chr4: 16685 SM1 Intergenic T C
homozygote
MACSNP015015522748 chr4: 16801 SM1 Intergenic C T
homozygote
MACSNP015015522758 chr4: 17184 SM1 Intergenic T C
homozygote
MACSNP015015522763 chr4: 17469 SM1 Intergenic G A
homozygote
MACSNP015015522785 chr4: 18174 SM1 Intergenic T C
homozygote
MACSNP015015522793 chr4: 18481 SM1 Intergenic A G
homozygote
MACSNP015015522796 chr4: 18548 SM1 Intergenic G T
homozygote
MACSNP015015522797 chr4: 18655 SM1 Intergenic A G
homozygote
MACSNP015015522808 chr4: 19220 SM1 Intergenic G C
homozygote

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