Variant report
Variant | rs2807661 |
---|---|
Chromosome Location | chr1:214773692-214773693 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000224584 | Chromatin interaction |
ENSG00000117724 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1467082 | 0.82[YRI][hapmap];1.00[AFR][1000 genomes] |
rs2457960 | 1.00[AMR][1000 genomes] |
rs2666832 | 0.82[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs2807666 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6697155 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1004475 | chr1:214763778-215013375 | Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |