Variant report
Variant | rs1756358 |
---|---|
Chromosome Location | chr14:83106846-83106847 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:2)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:2 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | STAT3 | chr14:83106666-83106964 | MCF10A-Er-Src | breast: | n/a | chr14:83106935-83106943 |
2 | POLR2A | chr14:83106682-83106882 | MCF10A-Er-Src | breast: | n/a | n/a |
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000258743 | TF binding region |
rs_ID | r2[population] |
---|---|
rs1756360 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2689119 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2798373 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2798374 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2798375 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2798378 | 0.86[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs7153004 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1054303 | chr14:83018016-83258920 | Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | esv2758364 | chr14:83035707-83146797 | Enhancers Active TSS Flanking Active TSS Weak transcription | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | esv2760002 | chr14:83035707-83146797 | Enhancers Active TSS Flanking Active TSS Weak transcription | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv2751286 | chr14:83066038-83203657 | Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |