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- rs11177217[chr12:68813366]
Enhancers that have rs11177217[chr12:68813366]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr12 |
68812065 |
68836135 |
enh14805 |
|
|
Transcript factors that have rs11177217[chr12:68813366]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr12
|
68813355
|
68813366
|
HOXA10
|
JASPAR
|
yes
|
|
121656026
|
|
|
chr12
|
68813356
|
68813366
|
ALX3
|
JASPAR
|
yes
|
|
121656027
|
|
|
chr12
|
68813356
|
68813366
|
EMX1
|
JASPAR
|
yes
|
|
121656028
|
|
|
chr12
|
68813356
|
68813366
|
EMX2
|
JASPAR
|
yes
|
|
121656029
|
|
|
chr12
|
68813356
|
68813366
|
ESX1
|
JASPAR
|
yes
|
|
121656030
|
|
|
chr12
|
68813356
|
68813366
|
GBX2
|
JASPAR
|
yes
|
|
121656031
|
|
|
chr12
|
68813356
|
68813366
|
GSX1
|
JASPAR
|
yes
|
|
121656032
|
|
|
chr12
|
68813356
|
68813366
|
GSX2
|
JASPAR
|
yes
|
|
121656033
|
|
|
chr12
|
68813356
|
68813366
|
HESX1
|
JASPAR
|
yes
|
|
121656034
|
|
|
chr12
|
68813356
|
68813366
|
HOXB2
|
JASPAR
|
yes
|
|
121656035
|
|
|
chr12
|
68813356
|
68813366
|
HOXB3
|
JASPAR
|
yes
|
|
121656036
|
|
|
chr12
|
68813356
|
68813366
|
LBX2
|
JASPAR
|
yes
|
|
121656037
|
|
|
chr12
|
68813356
|
68813366
|
LHX2
|
JASPAR
|
yes
|
|
121656038
|
|
|
chr12
|
68813356
|
68813366
|
LHX6
|
JASPAR
|
yes
|
|
121656039
|
|
|
chr12
|
68813356
|
68813366
|
MEOX1
|
JASPAR
|
yes
|
|
121656040
|
|
|
chr12
|
68813356
|
68813366
|
MEOX2
|
JASPAR
|
yes
|
|
121656041
|
|
|
chr12
|
68813356
|
68813366
|
MIXL1
|
JASPAR
|
yes
|
|
121656042
|
|
|
chr12
|
68813356
|
68813366
|
MNX1
|
JASPAR
|
yes
|
|
121656043
|
|
|
chr12
|
68813356
|
68813366
|
NOTO
|
JASPAR
|
yes
|
|
121656044
|
|
|
chr12
|
68813356
|
68813366
|
RAX
|
JASPAR
|
yes
|
|
121656045
|
|
|
chr12
|
68813357
|
68813367
|
POU6F2
|
JASPAR
|
yes
|
|
121656066
|
|
|
chr12
|
68813364
|
68813373
|
HIC2
|
JASPAR
|
yes
|
|
121656067
|
|
|
chr12
|
68813365
|
68813381
|
ZNF143
|
JASPAR
|
yes
|
|
121656068
|
|
|
chr12
|
68813366
|
68813376
|
SP1
|
JASPAR
|
yes
|
|
121656069
|
|
Genes associated with rs11177217[chr12:68813366], 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 |