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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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590414 SNVs 1 of 59042 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001000000013 chr1: 9666 CR1 Intergenic G C
heterozygote
MACSNP001000000021 chr1: 9800 CR1 Intergenic G C
heterozygote
MACSNP001000000051 chr1: 10493 CR1 Intergenic T C
heterozygote
MACSNP001000000052 chr1: 10504 CR1 Intergenic C T
heterozygote
MACSNP001000000056 chr1: 10569 CR1 Intergenic C T
heterozygote
MACSNP001000000060 chr1: 10630 CR1 Intergenic C T
heterozygote
MACSNP001000000070 chr1: 10885 CR1 Intergenic T C
homozygote
MACSNP001000000076 chr1: 10945 CR1 Intergenic G A
homozygote
MACSNP001000000087 chr1: 11183 CR1 Intergenic C A
heterozygote
MACSNP001000000089 chr1: 11245 CR1 Intergenic A C
homozygote

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