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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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504809 SNVs 1 of 50481 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP004026079082 chr6: 24174 TW1 Intergenic G T
heterozygote
MACSNP004026079091 chr6: 25120 TW1 Intergenic G C
heterozygote
MACSNP004026079107 chr6: 28178 TW1 Intergenic C T
homozygote
MACSNP004026079120 chr6: 31233 TW1 Intergenic T G
homozygote
MACSNP004026079143 chr6: 40999 TW1 Intergenic G C
homozygote
MACSNP004026079146 chr6: 41827 TW1 Intergenic C G
homozygote
MACSNP004026079149 chr6: 42774 TW1 Intergenic A C
homozygote
MACSNP004026079161 chr6: 44532 TW1 Intergenic G A
homozygote
MACSNP004026079178 chr6: 46945 TW1 Intergenic G A
homozygote
MACSNP004026079185 chr6: 47632 TW1 Intergenic C T
homozygote

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