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- SNP
- rs6945[chr19:2426828]
| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
Transcript factors that have rs6945[chr19:2426828]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
Genes associated with rs6945[chr19:2426828], 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 |
|
chr19
|
2425622
|
2427892
|
-
|
TIMM13
|
ENSG00000099800.3
|
2427892
|
0
|
Esophagus
|
2.80186e-35
|
16783
|
|
|
chr19
|
2425622
|
2427892
|
-
|
TIMM13
|
ENSG00000099800.3
|
2427892
|
0
|
Heart
|
1.56306e-06
|
16783
|
|
|
chr19
|
2425622
|
2427892
|
-
|
TIMM13
|
ENSG00000099800.3
|
2427892
|
0
|
Thyroid
|
3.33154e-13
|
16783
|
|