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- rs79959449[chr17:41776908]
Enhancers that have rs79959449[chr17:41776908]
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Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
chr17 |
41766774 |
41782454 |
enh32199 |
|
|
Transcript factors that have rs79959449[chr17:41776908]
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Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
chr17
|
41772237
|
41779348
|
ZBTB33
|
GTRD
|
no
|
Lung (A549)
|
108261567
|
|
chr17
|
41776452
|
41778958
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108261568
|
|
chr17
|
41776803
|
41778624
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21761464
|
|
chr17
|
41776905
|
41776917
|
MYBL1
|
JASPAR
|
yes
|
|
54368632
|
|
chr17
|
41776905
|
41776919
|
RXRB
|
JASPAR
|
yes
|
|
54368633
|
|
chr17
|
41776905
|
41776919
|
RXRG
|
JASPAR
|
yes
|
|
54368634
|
|
chr17
|
41776908
|
41776928
|
ESR1
|
JASPAR
|
yes
|
|
54368635
|
|
Genes associated with rs79959449[chr17:41776908], 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 |
chr17
|
41120105
|
41132545
|
-
|
PTGES3L
|
ENSG00000267060.1
|
41132545
|
644363
|
Esophagus
|
0.0909701
|
15887
|
|