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- rs2612067[chr12:66170163]
Enhancers that have rs2612067[chr12:66170163]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr12 |
66168947 |
66177881 |
enh58441 |
|
|
Transcript factors that have rs2612067[chr12:66170163]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr12
|
66168932
|
66170345
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553364
|
|
|
chr12
|
66169051
|
66170334
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553365
|
|
|
chr12
|
66169090
|
66170195
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553366
|
|
|
chr12
|
66169211
|
66170381
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553368
|
|
|
chr12
|
66169225
|
66170576
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553369
|
|
|
chr12
|
66169250
|
66170408
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553370
|
|
|
chr12
|
66169268
|
66170625
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553372
|
|
|
chr12
|
66169307
|
66170325
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553373
|
|
|
chr12
|
66169328
|
66170556
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553374
|
|
|
chr12
|
66169341
|
66170571
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553375
|
|
|
chr12
|
66169377
|
66170381
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553376
|
|
|
chr12
|
66169437
|
66170210
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553377
|
|
|
chr12
|
66169481
|
66170577
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21553378
|
|
|
chr12
|
66169800
|
66170377
|
P63
|
GTRD
|
no
|
Skin (Keratinocyte)
|
21553379
|
|
|
chr12
|
66170149
|
66170163
|
TCF7L2
|
JASPAR
|
yes
|
|
121492456
|
|
|
chr12
|
66170160
|
66170172
|
PBX1
|
JASPAR
|
yes
|
|
121492458
|
|
Genes associated with rs2612067[chr12:66170163], 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 |