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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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721909 SNVs 1 of 72191 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020056871533 chr14: 3954 BM1 Intergenic A G
homozygote
MACSNP020056871539 chr14: 4190 BM1 Intergenic G A
homozygote
MACSNP020056871541 chr14: 4326 BM1 Intergenic T C
homozygote
MACSNP020056871542 chr14: 4348 BM1 Intergenic A C
homozygote
MACSNP020056871551 chr14: 4684 BM1 Intergenic A T
homozygote
MACSNP020056871552 chr14: 4771 BM1 Intergenic G A
homozygote
MACSNP020056871559 chr14: 4939 BM1 Intergenic T C
homozygote
MACSNP020056871561 chr14: 4990 BM1 Intergenic C A
homozygote
MACSNP020056871572 chr14: 5523 BM1 Intergenic G A
homozygote
MACSNP020056871573 chr14: 5529 BM1 Intergenic G A
homozygote

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