Tag | Content |
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EnhancerAtlas ID | HS040-17383 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr19:534780-535830 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr19:535633-535644 | GGGTGACTCAG | + | 6.02 | JUN(var.2) | MA0489.1 | chr19:535302-535316 | CTGACTCATCCCCT | - | 6.04 | JUNB | MA0490.1 | chr19:535633-535644 | GGGTGACTCAG | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41993 | chr19:534817-536054 | LNCaP |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I000535 | chr19 | 535201 | 535270 |
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Enhancer Sequence | TGTCCAGACC TCGCCCATGA TCCAAGACCC CCGAGTGCCC TCCCTGTCCA GACCTCGCCC 60 ACGATCCAAG ACCCCCTGAG TGCCCTCCCT GTCCAGACCT CGCCCACGAT CCAAGACCCC 120 CTGAGTGCCC TCCCTGTCCA GGCTTCCACC ACGATCGCTC TGGGGGTGCT GCTCTCGTGC 180 CTTGGAGTGC TGAGTGCCAC CAGGACCCCT GACCCAGACA ACCTCTGTGT CTGGCACTGG 240 GGCCCAGCAG GAAAACAGTG AGGCTTCCTT GTTTACCTGC TGTGGCCCAG GAGGGCCGTG 300 GGTGGCATCA CGCCCCAGGC TGCAGGCCAG ACAGCTCTGT CACCTGGCAC GTGGCTTCAG 360 GCCTCCCTCT GTGGCCGTCC TTGCCAGCAG ATCTGGACCT CCAGGGCCTG GGTGACCACA 420 GGGGGCGATG CTGACAGGGA AGGAGTCCTG CCAGGTTTCT GTGACCTATG GGTCTGCCTG 480 CCTGACCCCC CAAGACCGGA CACCTGAGGG CAGACGGCCA TACTGACTCA TCCCCTCCCA 540 CGGCCTGGGC CAGGGCAGGT GTCACAAGTG TTTGCTAACT GAGCAATCAT CTGTGCTAAC 600 CCTCCCCACA CCCTGGCTGC CAAGGCCCTG GAGGTGCAGC CCTGGTCCTG GGCTTCAGCT 660 CCATCCAAGG GGAGCCTGGA GCCCCTGCCA GTCCATTCTG TCTGCTGGTG GGTGCCCCTG 720 GCCTGGGTCC CATATGCCTG ACCTGGGCTG CCACGGGCCT GGAGCCACGC GGGCAGCCAG 780 TGCCCACGTT CCCCAGCAGT TGTGCTGGGC CGGGTCCCGG CCACCTGGAC TGTGTAGGAG 840 CTGGGATCAG CTCGGGTGAC TCAGAAAAGG CTTCAGGCAG CCTTCTGGGG ACTTGACCCC 900 AGGCCTGTGA GAGTCCCTGC CTTGGGCAGG ATACGGTGTC CCTCACACAC ACCCTCAGGC 960 ACCAGCACTG GGAGTGGGAT GGCCTTGGGC ACCTTGTGAG CTGGGGCAGG TCTTGGGGCT 1020 GGGCTGGACT GAGCCACCTG CCTTCTGCCC 1050
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