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- rs1256500[chr14:65716967]
Enhancers that have rs1256500[chr14:65716967]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr14 |
65714905 |
65738715 |
enh15689 |
|
|
Transcript factors that have rs1256500[chr14:65716967]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr14
|
65716762
|
65717890
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21623822
|
|
|
chr14
|
65716783
|
65717904
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21623823
|
|
|
chr14
|
65716829
|
65717284
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21623824
|
|
|
chr14
|
65716911
|
65717486
|
SOX2
|
GTRD
|
no
|
Neural Stem Cells (H9)
|
21623825
|
|
|
chr14
|
65716921
|
65717142
|
SOX2
|
GTRD
|
no
|
Neural Stem Cells (H9)
|
21623826
|
|
|
chr14
|
65716923
|
65717245
|
SOX2
|
GTRD
|
no
|
Neural Stem Cells (H9)
|
21623827
|
|
|
chr14
|
65716958
|
65716975
|
ZNF410
|
JASPAR
|
yes
|
|
116048609
|
|
Genes associated with rs1256500[chr14:65716967], 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 |