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- rs140179231[chr17:39074728]
Enhancers that have rs140179231[chr17:39074728]
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Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
chr17 |
39055145 |
39077753 |
enh17145 |
|
|
Transcript factors that have rs140179231[chr17:39074728]
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Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
chr17
|
39074608
|
39074789
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21757289
|
|
chr17
|
39074727
|
39074739
|
NHLH1
|
JASPAR
|
yes
|
|
54244621
|
|
chr17
|
39074728
|
39074737
|
SNAI2
|
JASPAR
|
yes
|
|
54244622
|
|
chr17
|
39074728
|
39074738
|
ID4
|
JASPAR
|
yes
|
|
54244623
|
|
chr17
|
39074728
|
39074738
|
NHLH1
|
JASPAR
|
yes
|
|
54244624
|
|
chr17
|
39074728
|
39074738
|
TCF3
|
JASPAR
|
yes
|
|
54244625
|
|
chr17
|
39074728
|
39074738
|
TCF4
|
JASPAR
|
yes
|
|
54244626
|
|
Genes associated with rs140179231[chr17:39074728], 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
|
38544768
|
38574202
|
-
|
TOP2A
|
ENSG00000131747.10
|
38574202
|
500526
|
Esophagus
|
0.0511365
|
15767
|
|