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- rs79928669[chr11:16945316]
Enhancers that have rs79928669[chr11:16945316]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr11 |
16936985 |
16950715 |
enh13814 |
|
|
Transcript factors that have rs79928669[chr11:16945316]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr11
|
16945178
|
16945582
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21473387
|
|
|
chr11
|
16945178
|
16945582
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
107960575
|
|
|
chr11
|
16945274
|
16945597
|
ZNF274
|
GTRD
|
no
|
Liver (HepG2)
|
107960576
|
|
|
chr11
|
16945275
|
16947400
|
ZNF274
|
GTRD
|
no
|
Blood (GM12878)
|
107960577
|
|
|
chr11
|
16945306
|
16945316
|
SP1
|
JASPAR
|
yes
|
|
37688788
|
|
|
chr11
|
16945311
|
16945317
|
SP1
|
TRANSFAC
|
yes
|
|
37688789
|
|
|
chr11
|
16945315
|
16945326
|
NFIL3
|
JASPAR
|
yes
|
|
37688790
|
|
|
chr11
|
16945316
|
16945328
|
HLF
|
JASPAR
|
yes
|
|
37688791
|
|
Genes associated with rs79928669[chr11:16945316], 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 |