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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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261463 SNVs 1 of 26147 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007063857297 chr16: 997 CE1 Intergenic T C
heterozygote
MACSNP007063857301 chr16: 1077 CE1 Intergenic G C
heterozygote
MACSNP007063857309 chr16: 1242 CE1 Intergenic A C
heterozygote
MACSNP007063857310 chr16: 1260 CE1 Intergenic G T
heterozygote
MACSNP007063857311 chr16: 1303 CE1 Intergenic G C
heterozygote
MACSNP007063857315 chr16: 1369 CE1 Intergenic G A
heterozygote
MACSNP007063857328 chr16: 1903 CE1 Intergenic T C
heterozygote
MACSNP007063857334 chr16: 2246 CE1 Intergenic A G
heterozygote
MACSNP007063857335 chr16: 2264 CE1 Intergenic A G
heterozygote
MACSNP007063857338 chr16: 2378 CE1 Intergenic G A
heterozygote

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