Variant report
Variant | rs73160111 |
---|---|
Chromosome Location | chr3:17892935-17892936 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000131374 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11915290 | 0.86[AFR][1000 genomes] |
rs11918544 | 0.97[AFR][1000 genomes] |
rs11918876 | 0.90[AFR][1000 genomes] |
rs11925807 | 0.86[AFR][1000 genomes] |
rs57535465 | 0.86[AFR][1000 genomes] |
rs59925373 | 0.97[AFR][1000 genomes] |
rs61647180 | 0.86[AFR][1000 genomes] |
rs73160109 | 0.89[AFR][1000 genomes] |
rs73160120 | 0.97[AFR][1000 genomes] |
rs73160121 | 0.90[AFR][1000 genomes] |
rs73160145 | 0.97[AFR][1000 genomes] |
rs73160151 | 0.97[AFR][1000 genomes] |
rs73160153 | 0.97[AFR][1000 genomes] |
rs73160178 | 0.86[AFR][1000 genomes] |
rs73160182 | 0.97[AFR][1000 genomes] |
rs73160186 | 0.97[AFR][1000 genomes] |
rs73160188 | 0.87[AFR][1000 genomes] |
rs73160189 | 0.97[AFR][1000 genomes] |
rs73160201 | 0.93[AFR][1000 genomes] |
rs73171708 | 0.86[AFR][1000 genomes] |
rs73171709 | 0.86[AFR][1000 genomes] |
rs73171728 | 0.86[AFR][1000 genomes] |
rs73171737 | 0.86[AFR][1000 genomes] |
rs73171739 | 0.86[AFR][1000 genomes] |
rs73171744 | 0.86[AFR][1000 genomes] |
rs73171745 | 0.86[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv999594 | chr3:17690416-17982318 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:17891800-17893200 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
2 | chr3:17892800-17893000 | Enhancers | NHDF-Ad | bronchial |