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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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757221 SNVs 1 of 75723 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007000000070 chr1: 10885 CE1 Intergenic T C
homozygote
MACSNP007000000122 chr1: 12162 CE1 Intergenic A G
homozygote
MACSNP007000000140 chr1: 13625 CE1 Intergenic G A
homozygote
MACSNP007000000141 chr1: 13635 CE1 Intergenic T C
homozygote
MACSNP007000000146 chr1: 13826 CE1 Intergenic C T
homozygote
MACSNP007000000150 chr1: 13953 CE1 Intergenic G C
heterozygote
MACSNP007000000171 chr1: 14417 CE1 Intergenic C A
heterozygote
MACSNP007000000176 chr1: 14491 CE1 Intergenic G A
heterozygote
MACSNP007000000187 chr1: 14825 CE1 Intergenic C T
heterozygote
MACSNP007000000210 chr1: 15414 CE1 Intergenic T C
homozygote

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