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- rs12949135[chr17:39106013]
Enhancers that have rs12949135[chr17:39106013]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr17 |
39099743 |
39114455 |
enh17146 |
|
|
Transcript factors that have rs12949135[chr17:39106013]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr17
|
39105462
|
39106227
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21757322
|
|
|
chr17
|
39105600
|
39106126
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21757323
|
|
|
chr17
|
39105734
|
39106165
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21757324
|
|
|
chr17
|
39105817
|
39106153
|
ZNF274
|
ENCODE Uniform TFBS
|
no
|
Liver (HepG2)
|
21757325
|
|
|
chr17
|
39105856
|
39106060
|
ZNF274
|
ENCODE Uniform TFBS
|
no
|
Liver (HepG2)
|
21757326
|
|
|
chr17
|
39105878
|
39106058
|
ZNF274
|
ENCODE Uniform TFBS
|
no
|
Liver (HepG2)
|
21757327
|
|
|
chr17
|
39106003
|
39106024
|
ZNF263
|
JASPAR
|
yes
|
|
54246783
|
|
Genes associated with rs12949135[chr17:39106013], 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 |