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- rs113690386[chr17:49513444]
Enhancers that have rs113690386[chr17:49513444]
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Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
chr17 |
49502285 |
49519023 |
enh48044 |
|
|
Transcript factors that have rs113690386[chr17:49513444]
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Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
chr17
|
49511579
|
49515001
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
108272221
|
|
chr17
|
49511582
|
49514925
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
108272222
|
|
chr17
|
49512302
|
49514927
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
108272223
|
|
chr17
|
49512391
|
49513454
|
ZNF274
|
GTRD
|
no
|
Bone Marrow (K562)
|
108272225
|
|
chr17
|
49512428
|
49514454
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21772176
|
|
chr17
|
49512428
|
49514454
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108272226
|
|
chr17
|
49512444
|
49514954
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21772179
|
|
chr17
|
49512444
|
49514954
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108272229
|
|
chr17
|
49512469
|
49513689
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21772180
|
|
chr17
|
49512469
|
49513689
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108272230
|
|
chr17
|
49512828
|
49513501
|
ZNF274
|
GTRD
|
no
|
Blood (GM12878)
|
108272234
|
|
chr17
|
49512981
|
49513550
|
ZNF274
|
GTRD
|
no
|
Blood (GM12878)
|
108272238
|
|
chr17
|
49512990
|
49513466
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21772183
|
|
chr17
|
49512990
|
49513466
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108272239
|
|
chr17
|
49513016
|
49513586
|
ZNF217
|
ENCODE Uniform TFBS
|
no
|
Epithelial (MCF-7)
|
108272241
|
|
chr17
|
49513181
|
49515070
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21772185
|
|
chr17
|
49513181
|
49515070
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108272268
|
|
chr17
|
49513213
|
49513625
|
ZNF274
|
GTRD
|
no
|
Blood (GM12878)
|
108272271
|
|
chr17
|
49513442
|
49513463
|
IRF1
|
JASPAR
|
yes
|
|
54766726
|
|
chr17
|
49513444
|
49513459
|
FOXP1
|
JASPAR
|
yes
|
|
54766727
|
|
Genes associated with rs113690386[chr17:49513444], 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 |