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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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732061 SNVs 1 of 73207 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP019026079072 chr6: 22951 LM1 Intergenic G A
heterozygote
MACSNP019026079079 chr6: 24012 LM1 Intergenic T C
homozygote
MACSNP019026079087 chr6: 24550 LM1 Intergenic C A
homozygote
MACSNP019026079089 chr6: 24679 LM1 Intergenic G A
homozygote
MACSNP019026079090 chr6: 25025 LM1 Intergenic G C
homozygote
MACSNP019026079100 chr6: 26867 LM1 Intergenic G C
homozygote
MACSNP019026079107 chr6: 28178 LM1 Intergenic C T
homozygote
MACSNP019026079117 chr6: 30507 LM1 Intergenic G A
homozygote
MACSNP019026079127 chr6: 38929 LM1 Intergenic C T
homozygote
MACSNP019026079130 chr6: 39077 LM1 Intergenic T C
homozygote

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