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- rs182158697[chr12:45610965]
Enhancers that have rs182158697[chr12:45610965]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr12 |
45606948 |
45620795 |
enh14661 |
|
|
Transcript factors that have rs182158697[chr12:45610965]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr12
|
45610945
|
45610966
|
ZNF263
|
JASPAR
|
yes
|
|
120539361
|
|
|
chr12
|
45610948
|
45610969
|
ZNF263
|
JASPAR
|
yes
|
|
120539362
|
|
|
chr12
|
45610950
|
45610967
|
RXRA
|
JASPAR
|
yes
|
|
120539363
|
|
|
chr12
|
45610950
|
45610971
|
ZNF263
|
JASPAR
|
yes
|
|
120539364
|
|
|
chr12
|
45610953
|
45610974
|
ZNF263
|
JASPAR
|
yes
|
|
120539365
|
|
|
chr12
|
45610954
|
45610975
|
ZNF263
|
JASPAR
|
yes
|
|
120539368
|
|
|
chr12
|
45610956
|
45610971
|
PRDM1
|
JASPAR
|
yes
|
|
120539369
|
|
|
chr12
|
45610965
|
45610970
|
ETS2
|
TRANSFAC
|
yes
|
|
120539370
|
|
Genes associated with rs182158697[chr12:45610965], 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 |