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- rs4906037[chr14:101542480]
Enhancers that have rs4906037[chr14:101542480]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr14 |
101535911 |
101545535 |
enh31167 |
|
|
Transcript factors that have rs4906037[chr14:101542480]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr14
|
101542301
|
101542897
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21640534
|
|
|
chr14
|
101542427
|
101543545
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21640535
|
|
|
chr14
|
101542469
|
101542487
|
SRF
|
JASPAR
|
yes
|
|
117823731
|
|
|
chr14
|
101542474
|
101542484
|
NOTO
|
JASPAR
|
yes
|
|
117823732
|
|
|
chr14
|
101542474
|
101542486
|
SRF
|
JASPAR
|
yes
|
|
117823733
|
|
|
chr14
|
101542476
|
101542497
|
ZNF263
|
JASPAR
|
yes
|
|
117823734
|
|
|
chr14
|
101542480
|
101542501
|
ZNF263
|
JASPAR
|
yes
|
|
117823735
|
|
Genes associated with rs4906037[chr14:101542480], 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 |