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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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775202 SNVs 1 of 77521 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP008000000011 chr1: 9620 CE2 Intergenic C T
homozygote
MACSNP008000000015 chr1: 9719 CE2 Intergenic C T
heterozygote
MACSNP008000000021 chr1: 9800 CE2 Intergenic G C
homozygote
MACSNP008000000024 chr1: 9909 CE2 Intergenic T C
heterozygote
MACSNP008000000028 chr1: 9932 CE2 Intergenic T C
heterozygote
MACSNP008000000045 chr1: 10390 CE2 Intergenic T C
heterozygote
MACSNP008000000054 chr1: 10515 CE2 Intergenic G A
heterozygote
MACSNP008000000062 chr1: 10652 CE2 Intergenic G A
heterozygote
MACSNP008000000070 chr1: 10885 CE2 Intergenic T C
homozygote
MACSNP008000000098 chr1: 11493 CE2 Intergenic G A
heterozygote

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