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- rs183628659[chr16:89049987]
Enhancers that have rs183628659[chr16:89049987]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr16 |
89046288 |
89055611 |
enh47987 |
|
|
| chr16 |
89049819 |
89050070 |
vista23539 |
|
|
Transcript factors that have rs183628659[chr16:89049987]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr16
|
89047034
|
89056300
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224658
|
|
|
chr16
|
89047034
|
89056300
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224659
|
|
|
chr16
|
89047034
|
89056300
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224660
|
|
|
chr16
|
89047034
|
89056300
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224661
|
|
|
chr16
|
89047034
|
89056300
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224662
|
|
|
chr16
|
89047135
|
89056347
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224663
|
|
|
chr16
|
89047135
|
89056347
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224664
|
|
|
chr16
|
89047135
|
89056347
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224665
|
|
|
chr16
|
89047135
|
89056347
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224666
|
|
|
chr16
|
89047135
|
89056347
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224667
|
|
|
chr16
|
89047179
|
89056338
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224670
|
|
|
chr16
|
89047179
|
89056338
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224671
|
|
|
chr16
|
89047179
|
89056338
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224672
|
|
|
chr16
|
89047179
|
89056338
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224673
|
|
|
chr16
|
89047179
|
89056338
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224674
|
|
|
chr16
|
89049349
|
89050575
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224731
|
|
|
chr16
|
89049349
|
89050575
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224732
|
|
|
chr16
|
89049349
|
89050575
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224733
|
|
|
chr16
|
89049473
|
89050297
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224735
|
|
|
chr16
|
89049473
|
89050297
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224736
|
|
|
chr16
|
89049670
|
89050309
|
ZNF274
|
GTRD
|
no
|
Blood (GM12878)
|
108224737
|
|
|
chr16
|
89049670
|
89050309
|
ZNF274
|
GTRD
|
no
|
Blood (GM12878)
|
108224738
|
|
|
chr16
|
89049815
|
89050097
|
ZNF274
|
GTRD
|
no
|
Liver (HepG2)
|
108224739
|
|
|
chr16
|
89049881
|
89050121
|
ZZZ3
|
ENCODE Uniform TFBS
|
no
|
Blood (GM12878)
|
108224740
|
|
|
chr16
|
89049905
|
89055158
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224741
|
|
|
chr16
|
89049905
|
89055158
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224742
|
|
|
chr16
|
89049905
|
89055158
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108224743
|
|
|
chr16
|
89049980
|
89049988
|
WT1
|
TRANSFAC
|
yes
|
|
12313017
|
|
|
chr16
|
89049980
|
89049988
|
WT1
|
TRANSFAC
|
yes
|
|
49419869
|
|
|
chr16
|
89049983
|
89049993
|
SP1
|
JASPAR
|
yes
|
|
12313018
|
|
|
chr16
|
89049983
|
89049993
|
SP1
|
JASPAR
|
yes
|
|
49419870
|
|
|
chr16
|
89049985
|
89049996
|
ELK4
|
JASPAR
|
yes
|
|
12313019
|
|
|
chr16
|
89049985
|
89049996
|
FLI1
|
JASPAR
|
yes
|
|
12313020
|
|
|
chr16
|
89049985
|
89049996
|
ELK4
|
JASPAR
|
yes
|
|
49419871
|
|
|
chr16
|
89049985
|
89049996
|
FLI1
|
JASPAR
|
yes
|
|
49419872
|
|
Genes associated with rs183628659[chr16:89049987], 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 |