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- rs148893302[chr11:2099756]
Enhancers that have rs148893302[chr11:2099756]
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Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
chr11 |
2094981 |
2101122 |
enh28559 |
|
|
Transcript factors that have rs148893302[chr11:2099756]
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Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
chr11
|
2099368
|
2100257
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21466482
|
|
chr11
|
2099473
|
2100112
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21466483
|
|
chr11
|
2099489
|
2100121
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21466484
|
|
chr11
|
2099509
|
2100116
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21466485
|
|
chr11
|
2099511
|
2100050
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21466486
|
|
chr11
|
2099528
|
2100178
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21466487
|
|
chr11
|
2099542
|
2100114
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21466488
|
|
chr11
|
2099547
|
2100117
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21466489
|
|
chr11
|
2099572
|
2100268
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21466490
|
|
chr11
|
2099611
|
2100289
|
MYOD
|
GTRD
|
no
|
Muscle (Myoblast)
|
21466491
|
|
chr11
|
2099647
|
2100151
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21466492
|
|
chr11
|
2099687
|
2100055
|
ZNF274
|
GTRD
|
no
|
Liver (HepG2)
|
21466493
|
|
chr11
|
2099749
|
2099764
|
MEF2C
|
JASPAR
|
yes
|
|
36985016
|
|
chr11
|
2099750
|
2099762
|
MEF2A
|
JASPAR
|
yes
|
|
36985017
|
|
chr11
|
2099751
|
2099762
|
FOXC1
|
JASPAR
|
yes
|
|
36985018
|
|
chr11
|
2099752
|
2099756
|
YY1
|
TRANSFAC
|
yes
|
|
36985019
|
|
chr11
|
2099754
|
2099764
|
HOXA13
|
JASPAR
|
yes
|
|
36985020
|
|
chr11
|
2099754
|
2099764
|
HOXB13
|
JASPAR
|
yes
|
|
36985021
|
|
chr11
|
2099754
|
2099764
|
HOXD13
|
JASPAR
|
yes
|
|
36985022
|
|
chr11
|
2099754
|
2099765
|
HOXA10
|
JASPAR
|
yes
|
|
36985023
|
|
chr11
|
2099755
|
2099764
|
CDX1
|
JASPAR
|
yes
|
|
36985024
|
|
chr11
|
2099755
|
2099766
|
CDX2
|
JASPAR
|
yes
|
|
36985025
|
|
Genes associated with rs148893302[chr11:2099756], 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 |