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- rs900012[chr11:116966435]
Enhancers that have rs900012[chr11:116966435]
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Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
chr11 |
116958198 |
116967718 |
enh14305 |
|
|
Transcript factors that have rs900012[chr11:116966435]
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Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
chr11
|
116966418
|
116966435
|
RXRA
|
JASPAR
|
yes
|
|
41717768
|
|
chr11
|
116966428
|
116966438
|
MAX
|
JASPAR
|
yes
|
|
41717769
|
|
chr11
|
116966428
|
116966439
|
USF2
|
JASPAR
|
yes
|
|
41717770
|
|
chr11
|
116966428
|
116966440
|
HES7
|
JASPAR
|
yes
|
|
41717771
|
|
chr11
|
116966429
|
116966439
|
BHLHE40
|
JASPAR
|
yes
|
|
41717772
|
|
chr11
|
116966429
|
116966439
|
BHLHE41
|
JASPAR
|
yes
|
|
41717773
|
|
chr11
|
116966429
|
116966439
|
HEY1
|
JASPAR
|
yes
|
|
41717774
|
|
chr11
|
116966429
|
116966439
|
HEY2
|
JASPAR
|
yes
|
|
41717775
|
|
chr11
|
116966429
|
116966439
|
MAX
|
JASPAR
|
yes
|
|
41717776
|
|
chr11
|
116966429
|
116966439
|
MLXIPL
|
JASPAR
|
yes
|
|
41717777
|
|
chr11
|
116966429
|
116966439
|
MLX
|
JASPAR
|
yes
|
|
41717778
|
|
chr11
|
116966429
|
116966439
|
MNT
|
JASPAR
|
yes
|
|
41717779
|
|
chr11
|
116966429
|
116966439
|
SREBF2
|
JASPAR
|
yes
|
|
41717780
|
|
chr11
|
116966429
|
116966439
|
TFE3
|
JASPAR
|
yes
|
|
41717781
|
|
chr11
|
116966429
|
116966439
|
TFEB
|
JASPAR
|
yes
|
|
41717782
|
|
chr11
|
116966429
|
116966439
|
TFEC
|
JASPAR
|
yes
|
|
41717783
|
|
chr11
|
116966429
|
116966440
|
USF1
|
JASPAR
|
yes
|
|
41717784
|
|
chr11
|
116966429
|
116966440
|
USF2
|
JASPAR
|
yes
|
|
41717785
|
|
chr11
|
116966430
|
116966440
|
MAX
|
JASPAR
|
yes
|
|
41717786
|
|
chr11
|
116966431
|
116966436
|
MYC
|
TRANSFAC
|
yes
|
|
41717787
|
|
chr11
|
116966431
|
116966436
|
USF1
|
TRANSFAC
|
yes
|
|
41717788
|
|
chr11
|
116966431
|
116966436
|
USF2
|
TRANSFAC
|
yes
|
|
41717789
|
|
chr11
|
116966433
|
116966453
|
TBX19
|
JASPAR
|
yes
|
|
41717790
|
|
chr11
|
116966435
|
116966451
|
T
|
JASPAR
|
yes
|
|
41717791
|
|
Genes associated with rs900012[chr11:116966435], 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 |