Variant report
Variant | rs8017790 |
---|---|
Chromosome Location | chr14:56544200-56544201 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr14:56543596..56545113-chr5:172750348..172752553,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000113739 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10483662 | 1.00[EUR][1000 genomes] |
rs10498480 | 1.00[EUR][1000 genomes] |
rs10498482 | 1.00[EUR][1000 genomes] |
rs17090767 | 1.00[EUR][1000 genomes] |
rs17090780 | 1.00[EUR][1000 genomes] |
rs17090791 | 1.00[EUR][1000 genomes] |
rs17090840 | 1.00[EUR][1000 genomes] |
rs17090844 | 1.00[EUR][1000 genomes] |
rs17090848 | 1.00[EUR][1000 genomes] |
rs17090859 | 1.00[EUR][1000 genomes] |
rs2046095 | 0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58798057 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73287424 | 1.00[EUR][1000 genomes] |
rs73287467 | 0.83[AMR][1000 genomes] |
rs74051596 | 1.00[EUR][1000 genomes] |
rs74051597 | 1.00[EUR][1000 genomes] |
rs74051598 | 1.00[EUR][1000 genomes] |
rs74051599 | 1.00[EUR][1000 genomes] |
rs74051600 | 1.00[EUR][1000 genomes] |
rs74051601 | 1.00[EUR][1000 genomes] |
rs74051602 | 1.00[EUR][1000 genomes] |
rs74054303 | 1.00[EUR][1000 genomes] |
rs74054305 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv34106 | chr14:56346245-56550642 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:56541000-56554200 | Weak transcription | Gastric | stomach |