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- rs551096922[chr11:65184479]
Enhancers that have rs551096922[chr11:65184479]
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Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
chr11 |
65180298 |
65217415 |
enh1825 |
|
|
Transcript factors that have rs551096922[chr11:65184479]
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Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
chr11
|
65180596
|
65184873
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21491469
|
|
chr11
|
65180736
|
65184733
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21491491
|
|
chr11
|
65183437
|
65204678
|
POLR2A
|
UCSC Txn Factor
|
no
|
Conserved
|
107977988
|
|
chr11
|
65183437
|
65204678
|
POLR2A
|
UCSC Txn Factor
|
no
|
Conserved
|
107977989
|
|
chr11
|
65183437
|
65204678
|
POLR2A
|
UCSC Txn Factor
|
no
|
Conserved
|
107977990
|
|
chr11
|
65183972
|
65184655
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21491674
|
|
chr11
|
65184002
|
65184676
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21491675
|
|
chr11
|
65184054
|
65184548
|
SOX2
|
GTRD
|
no
|
Neural Stem Cells (H9)
|
21491678
|
|
chr11
|
65184061
|
65184542
|
SOX2
|
GTRD
|
no
|
Neural Stem Cells (H9)
|
21491679
|
|
chr11
|
65184077
|
65184845
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21491680
|
|
chr11
|
65184092
|
65184662
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21491681
|
|
chr11
|
65184095
|
65184699
|
ZZZ3
|
ENCODE Uniform TFBS
|
no
|
Cervix (HeLa-S3)
|
21491682
|
|
chr11
|
65184102
|
65184608
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21491683
|
|
chr11
|
65184122
|
65184522
|
ZZZ3
|
ENCODE Uniform TFBS
|
no
|
Blood (GM12878)
|
21491684
|
|
chr11
|
65184125
|
65184622
|
SOX2
|
GTRD
|
no
|
Neural Stem Cells (H9)
|
21491685
|
|
chr11
|
65184228
|
65184748
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21491686
|
|
chr11
|
65184473
|
65184490
|
RXRA
|
JASPAR
|
yes
|
|
39313393
|
|
chr11
|
65184476
|
65184491
|
HNF4A
|
JASPAR
|
yes
|
|
39313394
|
|
chr11
|
65184477
|
65184492
|
HNF4G
|
JASPAR
|
yes
|
|
39313395
|
|
chr11
|
65184477
|
65184492
|
NR2C2
|
JASPAR
|
yes
|
|
39313396
|
|
Genes associated with rs551096922[chr11:65184479], 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 |