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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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1020935 SNVs 1 of 102094 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020026079056 chr6: 12242 BM1 Intergenic C A
heterozygote
MACSNP020026079065 chr6: 17502 BM1 Intergenic C T
heterozygote
MACSNP020026079078 chr6: 23940 BM1 Intergenic A G
homozygote
MACSNP020026079079 chr6: 24012 BM1 Intergenic T C
homozygote
MACSNP020026079090 chr6: 25025 BM1 Intergenic G C
homozygote
MACSNP020026079100 chr6: 26867 BM1 Intergenic G C
homozygote
MACSNP020026079102 chr6: 27355 BM1 Intergenic T G
homozygote
MACSNP020026079103 chr6: 27484 BM1 Intergenic C T
heterozygote
MACSNP020026079127 chr6: 38929 BM1 Intergenic C T
homozygote
MACSNP020026079130 chr6: 39077 BM1 Intergenic T C
homozygote

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