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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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715973 SNVs 1 of 71598 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016000000001 chr1: 9299 SM2 Intergenic G C
heterozygote
MACSNP016000000012 chr1: 9645 SM2 Intergenic C T
homozygote
MACSNP016000000014 chr1: 9668 SM2 Intergenic G A
homozygote
MACSNP016000000015 chr1: 9719 SM2 Intergenic C T
homozygote
MACSNP016000000041 chr1: 10358 SM2 Intergenic C T
heterozygote
MACSNP016000000051 chr1: 10493 SM2 Intergenic T C
heterozygote
MACSNP016000000070 chr1: 10885 SM2 Intergenic T C
homozygote
MACSNP016000000074 chr1: 10926 SM2 Intergenic C T
homozygote
MACSNP016000000076 chr1: 10945 SM2 Intergenic G A
homozygote
MACSNP016000000077 chr1: 10979 SM2 Intergenic G C
homozygote

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