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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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394139 SNVs 1 of 39414 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001040365706 chr9: 3205 CR1 Intergenic A G
homozygote
MACSNP001040365718 chr9: 3984 CR1 Intergenic A G
homozygote
MACSNP001040365750 chr9: 8712 CR1 Intergenic C T
homozygote
MACSNP001040365770 chr9: 12463 CR1 Intergenic T G
homozygote
MACSNP001040365772 chr9: 12550 CR1 Intergenic T C
homozygote
MACSNP001040365773 chr9: 13037 CR1 Intergenic G C
homozygote
MACSNP001040365787 chr9: 14278 CR1 Intergenic G A
homozygote
MACSNP001040365795 chr9: 14439 CR1 Intergenic G A
homozygote
MACSNP001040365814 chr9: 14929 CR1 Intergenic G C
heterozygote
MACSNP001040365815 chr9: 14957 CR1 Intergenic A C
heterozygote

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