Variant report
Variant | rs6923998 |
---|---|
Chromosome Location | chr6:54825709-54825710 |
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:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000261235 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs16886099 | 1.00[EUR][1000 genomes] |
rs3105260 | 1.00[EUR][1000 genomes] |
rs57915824 | 1.00[EUR][1000 genomes] |
rs58658626 | 1.00[EUR][1000 genomes] |
rs59536488 | 1.00[EUR][1000 genomes] |
rs59630560 | 1.00[EUR][1000 genomes] |
rs73434487 | 1.00[EUR][1000 genomes] |
rs73438551 | 1.00[EUR][1000 genomes] |
rs73438552 | 1.00[EUR][1000 genomes] |
rs73438561 | 1.00[EUR][1000 genomes] |
rs7356813 | 1.00[EUR][1000 genomes] |
rs7740224 | 1.00[EUR][1000 genomes] |
rs7762218 | 1.00[EUR][1000 genomes] |
rs7766442 | 1.00[EUR][1000 genomes] |
rs9475055 | 1.00[EUR][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 |
No data |