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- rs117729444[chr11:2049281]
Enhancers that have rs117729444[chr11:2049281]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr11 |
2049072 |
2053176 |
enh43474 |
|
|
Transcript factors that have rs117729444[chr11:2049281]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr11
|
2049271
|
2049286
|
NFYB
|
JASPAR
|
yes
|
|
36982946
|
|
|
chr11
|
2049273
|
2049289
|
NFYA
|
JASPAR
|
yes
|
|
36982947
|
|
|
chr11
|
2049274
|
2049292
|
NFYA
|
JASPAR
|
yes
|
|
36982949
|
|
|
chr11
|
2049277
|
2049287
|
EN2
|
JASPAR
|
yes
|
|
36982950
|
|
|
chr11
|
2049278
|
2049282
|
H1TF2
|
TRANSFAC
|
yes
|
|
36982951
|
|
|
chr11
|
2049278
|
2049282
|
NFE
|
TRANSFAC
|
yes
|
|
36982952
|
|
|
chr11
|
2049278
|
2049282
|
SRF
|
TRANSFAC
|
yes
|
|
36982953
|
|
Genes associated with rs117729444[chr11:2049281], 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 |
|
chr11
|
1773982
|
1785222
|
-
|
CTSD
|
ENSG00000117984.8
|
1785222
|
264059
|
Esophagus
|
0.334342
|
10401
|
|
|
chr11
|
1860219
|
1862910
|
+
|
TNNI2
|
ENSG00000130598.11
|
1860219
|
186371
|
Uterus
|
0.322567
|
10403
|
|