Variant report
Variant | rs12133443 |
---|---|
Chromosome Location | chr1:104791114-104791115 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11185410 | 0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12129522 | 0.86[AFR][1000 genomes] |
rs12130258 | 0.86[AFR][1000 genomes] |
rs12406466 | 0.88[AFR][1000 genomes] |
rs12406661 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12407649 | 0.85[ASN][1000 genomes] |
rs1497679 | 0.86[AFR][1000 genomes] |
rs2209954 | 0.81[AFR][1000 genomes] |
rs2317080 | 0.88[AFR][1000 genomes] |
rs2317081 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2873357 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4325136 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4571975 | 0.86[AFR][1000 genomes] |
rs5001661 | 0.86[AFR][1000 genomes] |
rs56868860 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6586449 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6586450 | 0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6667359 | 0.88[AFR][1000 genomes] |
rs6675138 | 0.84[AFR][1000 genomes] |
rs6675141 | 0.86[AFR][1000 genomes] |
rs967982 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv872072 | chr1:104470622-105076810 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv1010903 | chr1:104483363-105468941 | Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv823764 | chr1:104791021-104791955 | Enhancers | n/a | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:104791000-104791200 | Enhancers | Fetal Lung | lung |