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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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634306 SNVs 1 of 63431 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010031370899 chr7: 19035 CE4 Intergenic C T
heterozygote
MACSNP010031370901 chr7: 19043 CE4 Intergenic C G
heterozygote
MACSNP010031370930 chr7: 25705 CE4 Intergenic T G
homozygote
MACSNP010031370936 chr7: 25961 CE4 Intergenic G A
homozygote
MACSNP010031370938 chr7: 26115 CE4 Intergenic G T
homozygote
MACSNP010031370963 chr7: 28309 CE4 Intergenic C G
heterozygote
MACSNP010031370975 chr7: 28771 CE4 Intergenic T C
homozygote
MACSNP010031370976 chr7: 28814 CE4 Intergenic G A
heterozygote
MACSNP010031371008 chr7: 29877 CE4 Intergenic T C
heterozygote
MACSNP010031371013 chr7: 30573 CE4 Intergenic G A
heterozygote

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