Variant report
Variant | rs4652420 |
---|---|
Chromosome Location | chr1:179562143-179562144 |
allele | A/G |
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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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000227141 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10157699 | 1.00[CHB][hapmap];0.84[JPT][hapmap];0.93[ASN][1000 genomes] |
rs10798708 | 1.00[CHB][hapmap];0.83[CHD][hapmap];0.88[GIH][hapmap];0.86[JPT][hapmap] |
rs10913847 | 0.82[CHB][hapmap];0.83[JPT][hapmap] |
rs12042786 | 0.84[EUR][1000 genomes] |
rs1410594 | 1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap] |
rs1590783 | 0.91[ASN][1000 genomes] |
rs3930537 | 1.00[CHB][hapmap];0.94[GIH][hapmap];0.85[TSI][hapmap] |
rs4443850 | 1.00[CHB][hapmap];0.86[JPT][hapmap] |
rs4628468 | 1.00[CHB][hapmap];0.83[CHD][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes] |
rs4652418 | 1.00[ASN][1000 genomes] |
rs6700202 | 0.83[EUR][1000 genomes] |
rs7534216 | 1.00[CHB][hapmap];0.83[CHD][hapmap];0.88[GIH][hapmap];0.86[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3424735 | chr1:179559954-179562502 | Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |