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- rs4902633[chr14:69181968]
Enhancers that have rs4902633[chr14:69181968]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr14 |
69167794 |
69210979 |
enh15721 |
|
|
| chr14 |
69181651 |
69182330 |
vista18261 |
|
|
Transcript factors that have rs4902633[chr14:69181968]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr14
|
69181422
|
69182064
|
ZNF274
|
GTRD
|
no
|
Liver (HepG2)
|
108110319
|
|
|
chr14
|
69181583
|
69181973
|
ZNF274
|
ENCODE Uniform TFBS
|
no
|
Bone Marrow (K562)
|
21625737
|
|
|
chr14
|
69181583
|
69181973
|
ZNF274
|
ENCODE Uniform TFBS
|
no
|
Bone Marrow (K562)
|
108110320
|
|
|
chr14
|
69181955
|
69181975
|
PPARG
|
JASPAR
|
yes
|
|
107572388
|
|
|
chr14
|
69181955
|
69181975
|
PPARG
|
JASPAR
|
yes
|
|
116250349
|
|
|
chr14
|
69181956
|
69181970
|
JUN
|
JASPAR
|
yes
|
|
107572392
|
|
|
chr14
|
69181956
|
69181970
|
JUN
|
JASPAR
|
yes
|
|
116250353
|
|
Genes associated with rs4902633[chr14:69181968], 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 |