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- SNP
- rs9697358[chr1:947778]
| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
Transcript factors that have rs9697358[chr1:947778]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr1
|
934818
|
949157
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
107801762
|
|
|
chr1
|
934818
|
949157
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
107801763
|
|
|
chr1
|
934818
|
949157
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
107801764
|
|
Genes associated with rs9697358[chr1:947778], 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 |
|
chr1
|
1470554
|
1475833
|
-
|
TMEM240
|
ENSG00000205090.4
|
1475833
|
522776
|
Stomach
|
0.0839223
|
41
|
|