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- rs4905985[chr14:101111349]
Enhancers that have rs4905985[chr14:101111349]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr14 |
101102755 |
101149275 |
enh15944 |
|
|
Transcript factors that have rs4905985[chr14:101111349]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr14
|
101110909
|
101113521
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21639470
|
|
|
chr14
|
101111096
|
101111466
|
ZNF274
|
ENCODE Uniform TFBS
|
no
|
Bone Marrow (K562)
|
21639471
|
|
|
chr14
|
101111139
|
101111415
|
ZNF274
|
ENCODE Uniform TFBS
|
no
|
Bone Marrow (K562)
|
21639472
|
|
|
chr14
|
101111304
|
101112010
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21639474
|
|
|
chr14
|
101111348
|
101111353
|
SP1
|
TRANSFAC
|
yes
|
|
117788639
|
|
|
chr14
|
101111348
|
101111363
|
HNF4A
|
JASPAR
|
yes
|
|
117788640
|
|
|
chr14
|
101111349
|
101111363
|
NR2F1
|
JASPAR
|
yes
|
|
117788641
|
|
|
chr14
|
101111349
|
101111364
|
HNF4G
|
JASPAR
|
yes
|
|
117788642
|
|
Genes associated with rs4905985[chr14:101111349], 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 |