Variant report
Variant | rs7155646 |
---|---|
Chromosome Location | chr14:80278006-80278007 |
allele | C/G |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs11628399 | 1.00[ASN][1000 genomes] |
rs11628915 | 0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12586263 | 0.87[ASN][1000 genomes] |
rs12586501 | 1.00[ASN][1000 genomes] |
rs12588661 | 1.00[ASN][1000 genomes] |
rs12588956 | 0.93[ASN][1000 genomes] |
rs12589656 | 0.90[ASN][1000 genomes] |
rs12590090 | 0.93[ASN][1000 genomes] |
rs12590550 | 0.93[ASN][1000 genomes] |
rs12881435 | 0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17174723 | 0.87[ASN][1000 genomes] |
rs17764518 | 0.87[ASN][1000 genomes] |
rs17764884 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs34549185 | 0.97[ASN][1000 genomes] |
rs34764611 | 0.83[ASN][1000 genomes] |
rs35224540 | 0.82[EUR][1000 genomes] |
rs35732569 | 0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs56122467 | 0.87[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs67488951 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs7158292 | 0.87[ASN][1000 genomes] |
rs72696796 | 0.87[ASN][1000 genomes] |
rs72698405 | 1.00[ASN][1000 genomes] |
rs8021767 | 0.90[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1045241 | chr14:79885361-80734201 | Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
2 | nsv902113 | chr14:80172094-80929699 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:80277000-80280400 | Weak transcription | Brain Inferior Temporal Lobe | brain |