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- SNP
- rs9691628[chr7:542550]
| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr7 |
540425 |
549795 |
enh56132 |
|
|
Transcript factors that have rs9691628[chr7:542550]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr7
|
542541
|
542561
|
RREB1
|
JASPAR
|
yes
|
|
12400748
|
|
|
chr7
|
542542
|
542552
|
ZNF740
|
JASPAR
|
yes
|
|
12400749
|
|
|
chr7
|
542542
|
542556
|
GLIS2
|
JASPAR
|
yes
|
|
12400750
|
|
Genes associated with rs9691628[chr7:542550], comfirmed by eQTL
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Blank TSI value indicates lack of sufficient expression for calculation
| Chrom. |
Start |
End |
Strand |
Gene name |
Ensembl ID |
TSS of gene |
Distance between TSS and SNP |
Tissue |
q Value |
id |
More |
|
chr7
|
536895
|
559933
|
-
|
PDGFA
|
ENSG00000197461.9
|
559933
|
0
|
Esophagus
|
0.000241533
|
7149
|
|