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- SNP
- rs6950[chr16:30995669]
| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
Transcript factors that have rs6950[chr16:30995669]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr16
|
30994267
|
30997602
|
ZNF274
|
GTRD
|
no
|
Blood (GM12878)
|
108192761
|
|
Genes associated with rs6950[chr16:30995669], 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 |
|
chr16
|
30996519
|
31000473
|
+
|
HSD3B7
|
ENSG00000099377.9
|
30996519
|
850
|
Esophagus
|
5.72361e-38
|
14769
|
|