Variant report
Variant | rs17107106 |
---|---|
Chromosome Location | chr14:38260034-38260035 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:1 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | FOXA2 | chr14:38259595-38262168 | HepG2 | liver: | n/a | chr14:38260697-38260709 |
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
TTC6 | TF binding region |
rs_ID | r2[population] |
---|---|
rs11849079 | 0.83[CEU][hapmap];1.00[CHB][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12587895 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs12590844 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs17107096 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs17107102 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[CHD][hapmap];0.84[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs17107141 | 0.85[CEU][hapmap];1.00[CHB][hapmap];0.81[CHD][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.92[TSI][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1951645 | 0.89[CEU][hapmap];0.88[EUR][1000 genomes] |
rs1952784 | 0.80[CEU][hapmap];0.96[TSI][hapmap];0.83[EUR][1000 genomes] |
rs1957584 | 0.94[CEU][hapmap];0.90[EUR][1000 genomes] |
rs1980680 | 0.89[CEU][hapmap];0.88[EUR][1000 genomes] |
rs2415414 | 0.89[EUR][1000 genomes] |
rs4901274 | 0.94[CEU][hapmap];0.90[EUR][1000 genomes] |
rs55712036 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs58878623 | 0.92[EUR][1000 genomes] |
rs59262826 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs61977158 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs66496750 | 0.95[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs66617416 | 0.95[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs67863208 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs726238 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs8010511 | 0.90[EUR][1000 genomes] |
rs8011077 | 0.94[CEU][hapmap];0.89[EUR][1000 genomes] |
rs8012810 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs969446 | 0.94[CEU][hapmap];0.96[TSI][hapmap];0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530038 | chr14:37590543-38336191 | Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 58 gene(s) | inside rSNPs | diseases |
2 | nsv916985 | chr14:38052347-38838551 | Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 59 gene(s) | inside rSNPs | diseases |
3 | nsv564383 | chr14:38223275-38262762 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers | TF binding regionCpG island | 1 gene(s) | inside rSNPs | diseases |
4 | nsv564384 | chr14:38233493-38262762 | Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers | TF binding regionCpG island | 1 gene(s) | inside rSNPs | diseases |
5 | nsv564385 | chr14:38246440-38321607 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:38259400-38261600 | Enhancers | HepG2 | liver |