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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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747438 SNVs 1 of 74744 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011020528809 chr5: 323 CE5 Intergenic G A
heterozygote
MACSNP011020528851 chr5: 20860 CE5 Intergenic C T
heterozygote
MACSNP011020528852 chr5: 21121 CE5 Intergenic T C
heterozygote
MACSNP011020528854 chr5: 21282 CE5 Intergenic T C
heterozygote
MACSNP011020528859 chr5: 21488 CE5 Intergenic A G
heterozygote
MACSNP011020528860 chr5: 21512 CE5 Intergenic T C
heterozygote
MACSNP011020528861 chr5: 21534 CE5 Intergenic G A
homozygote
MACSNP011020528875 chr5: 23394 CE5 Intergenic G A
homozygote
MACSNP011020528876 chr5: 23404 CE5 Intergenic A G
heterozygote
MACSNP011020528897 chr5: 24823 CE5 Intergenic G A
heterozygote

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