Variant report
Variant | rs1457052 |
---|---|
Chromosome Location | chr8:92605773-92605774 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:1 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
RN7SKP231 | TF binding region |
rs_ID | r2[population] |
---|---|
rs11986042 | 1.00[CEU][hapmap] |
rs28735086 | 0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs56160120 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs56318259 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs57453564 | 0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs57610492 | 0.89[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs58830410 | 0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs58888435 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs59075912 | 0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73309604 | 0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs73309653 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73309657 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73309674 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7832321 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9649975 | 0.92[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1029962 | chr8:92560661-92753342 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv831391 | chr8:92578256-92761091 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |