-
Home
- SNP
- rs139617259[chr17:49517038]
Enhancers that have rs139617259[chr17:49517038]
Back to top
| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr17 |
49502285 |
49519023 |
enh48044 |
|
|
Transcript factors that have rs139617259[chr17:49517038]
Back to top
| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr17
|
49515125
|
49517143
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21772192
|
|
|
chr17
|
49516069
|
49517293
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21772197
|
|
|
chr17
|
49517036
|
49517047
|
ELK4
|
JASPAR
|
yes
|
|
54767239
|
|
|
chr17
|
49517036
|
49517047
|
FLI1
|
JASPAR
|
yes
|
|
54767240
|
|
|
chr17
|
49517037
|
49517047
|
ERG
|
JASPAR
|
yes
|
|
54767241
|
|
|
chr17
|
49517037
|
49517047
|
ETS1
|
JASPAR
|
yes
|
|
54767242
|
|
|
chr17
|
49517037
|
49517047
|
FLI1
|
JASPAR
|
yes
|
|
54767243
|
|
|
chr17
|
49517037
|
49517048
|
ETV2
|
JASPAR
|
yes
|
|
54767244
|
|
Genes associated with rs139617259[chr17:49517038], comfirmed by eQTL
Back to top
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 |