Variant report
Variant | rs6933826 |
---|---|
Chromosome Location | chr6:54626645-54626646 |
allele | C/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 |
---|---|
ENSG00000168143 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs16885860 | 1.00[AMR][1000 genomes] |
rs16885898 | 1.00[AMR][1000 genomes] |
rs56762989 | 1.00[AMR][1000 genomes] |
rs6909009 | 1.00[AMR][1000 genomes] |
rs6909061 | 1.00[AMR][1000 genomes] |
rs73743467 | 1.00[AMR][1000 genomes] |
rs7758802 | 1.00[AMR][1000 genomes] |
rs7776195 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv885900 | chr6:54517968-54852462 | Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | nsv885901 | chr6:54588069-54635417 | Enhancers Weak transcription Strong transcription Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv885902 | chr6:54588069-54656673 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |