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- SNP
- rs1069[chr17:59574598]
| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr17 |
59564765 |
59575175 |
enh32254 |
|
|
Transcript factors that have rs1069[chr17:59574598]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr17
|
59574522
|
59574731
|
ZNF274
|
ENCODE Uniform TFBS
|
no
|
Liver (HepG2)
|
21777472
|
|
|
chr17
|
59574562
|
59574710
|
ZNF274
|
ENCODE Uniform TFBS
|
no
|
Liver (HepG2)
|
21777473
|
|
Genes associated with rs1069[chr17:59574598], 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
|
60536019
|
60692842
|
+
|
TLK2
|
ENSG00000146872.13
|
60536019
|
961421
|
Esophagus
|
0.224674
|
16129
|
|