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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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571095 SNVs 1 of 57110 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001026079079 chr6: 24012 CR1 Intergenic T C
heterozygote
MACSNP001026079107 chr6: 28178 CR1 Intergenic C T
homozygote
MACSNP001026079120 chr6: 31233 CR1 Intergenic T G
homozygote
MACSNP001026079124 chr6: 38526 CR1 Intergenic C A
heterozygote
MACSNP001026079136 chr6: 39640 CR1 Intergenic A T
heterozygote
MACSNP001026079138 chr6: 39787 CR1 Intergenic C A
homozygote
MACSNP001026079149 chr6: 42774 CR1 Intergenic A C
homozygote
MACSNP001026079161 chr6: 44532 CR1 Intergenic G A
homozygote
MACSNP001026079178 chr6: 46945 CR1 Intergenic G A
homozygote
MACSNP001026079184 chr6: 47616 CR1 Intergenic A G
heterozygote

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