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- rs569770597[chr7:408996]
Enhancers that have rs569770597[chr7:408996]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr7 |
387285 |
423895 |
enh23904 |
|
|
Transcript factors that have rs569770597[chr7:408996]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr7
|
408983
|
408998
|
TFAP2C
|
JASPAR
|
yes
|
|
12388360
|
|
|
chr7
|
408986
|
408997
|
TFAP2A
|
JASPAR
|
yes
|
|
12388361
|
|
|
chr7
|
408986
|
408997
|
TFAP2B
|
JASPAR
|
yes
|
|
12388362
|
|
|
chr7
|
408986
|
408997
|
TFAP2C
|
JASPAR
|
yes
|
|
12388363
|
|
|
chr7
|
408994
|
409013
|
REST
|
JASPAR
|
yes
|
|
12388364
|
|
|
chr7
|
408996
|
409007
|
TFAP2A
|
JASPAR
|
yes
|
|
12388365
|
|
|
chr7
|
408996
|
409007
|
TFAP2B
|
JASPAR
|
yes
|
|
12388366
|
|
|
chr7
|
408996
|
409008
|
TFAP2A
|
JASPAR
|
yes
|
|
12388367
|
|
Genes associated with rs569770597[chr7:408996], 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 |