Variant report
Variant | rs7136525 |
---|---|
Chromosome Location | chr12:56253209-56253210 |
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:
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Variant related genes | Relation type |
---|---|
ENSG00000065357 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1066130 | 1.00[ASN][1000 genomes] |
rs1068189 | 1.00[ASN][1000 genomes] |
rs2658478 | 1.00[ASN][1000 genomes] |
rs772459 | 1.00[ASN][1000 genomes] |
rs772470 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832423 | chr12:56080822-56253698 | Flanking Active TSS Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 119 gene(s) | inside rSNPs | diseases |
2 | nsv719 | chr12:56246405-56290812 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
3 | nsv508675 | chr12:56249598-56260508 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |