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- rs185593871[chr12:65996684]
Enhancers that have rs185593871[chr12:65996684]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr12 |
65985125 |
66011195 |
enh47591 |
|
|
Transcript factors that have rs185593871[chr12:65996684]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr12
|
65995955
|
65996966
|
P63
|
GTRD
|
no
|
Skin (Keratinocyte)
|
21553120
|
|
|
chr12
|
65996042
|
65996857
|
P63
|
GTRD
|
no
|
Skin (Keratinocyte)
|
21553121
|
|
|
chr12
|
65996386
|
65996696
|
ZNF217
|
ENCODE Uniform TFBS
|
no
|
Epithelial (MCF-7)
|
21553129
|
|
|
chr12
|
65996564
|
65996894
|
ZZZ3
|
ENCODE Uniform TFBS
|
no
|
Cervix (HeLa-S3)
|
21553131
|
|
|
chr12
|
65996594
|
65996733
|
ZBTB33
|
ENCODE Uniform TFBS
|
no
|
Colon (HCT116)
|
21553132
|
|
|
chr12
|
65996630
|
65997094
|
ZBTB33
|
ENCODE Uniform TFBS
|
no
|
Colon (HCT116)
|
21553133
|
|
Genes associated with rs185593871[chr12:65996684], 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 |