Variant report
Variant | rs72918771 |
---|---|
Chromosome Location | chr4:100977584-100977585 |
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 |
---|---|
ENSG00000245322 | Chromatin interaction |
ENSG00000164032 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs57427258 | 1.00[AFR][1000 genomes] |
rs6833047 | 1.00[AFR][1000 genomes] |
rs72913042 | 1.00[AFR][1000 genomes] |
rs72918775 | 1.00[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv427689 | chr4:100931741-101216531 | Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv830018 | chr4:100977238-101027920 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |