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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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682034 SNVs 1 of 68204 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007015522748 chr4: 16801 CE1 Intergenic C T
homozygote
MACSNP007015522756 chr4: 17080 CE1 Intergenic G A
homozygote
MACSNP007015522758 chr4: 17184 CE1 Intergenic T C
homozygote
MACSNP007015522761 chr4: 17366 CE1 Intergenic G A
homozygote
MACSNP007015522763 chr4: 17469 CE1 Intergenic G A
homozygote
MACSNP007015522785 chr4: 18174 CE1 Intergenic T C
homozygote
MACSNP007015522793 chr4: 18481 CE1 Intergenic A G
homozygote
MACSNP007015522808 chr4: 19220 CE1 Intergenic G C
homozygote
MACSNP007015522825 chr4: 19703 CE1 Intergenic T A
homozygote
MACSNP007015522826 chr4: 19818 CE1 Intergenic G T
homozygote

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