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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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911793 SNVs 1 of 91180 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020031370930 chr7: 25705 BM1 Intergenic T G
homozygote
MACSNP020031370954 chr7: 27751 BM1 Intergenic C G
homozygote
MACSNP020031370956 chr7: 27775 BM1 Intergenic C A
homozygote
MACSNP020031370957 chr7: 27795 BM1 Intergenic G A
homozygote
MACSNP020031370960 chr7: 27990 BM1 Intergenic C T
homozygote
MACSNP020031370983 chr7: 29177 BM1 Intergenic C A
homozygote
MACSNP020031370989 chr7: 29282 BM1 Intergenic G T
homozygote
MACSNP020031370999 chr7: 29553 BM1 Intergenic T C
homozygote
MACSNP020031371005 chr7: 29855 BM1 Intergenic A T
homozygote
MACSNP020031371054 chr7: 33687 BM1 Intergenic G A
heterozygote

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