Tag | Content |
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EnhancerAtlas ID | HS040-34752 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr9:95749830-95751200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP53 | MA0106.3 | chr9:95750617-95750635 | GGCATGCCCAGGCAAGAC | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_18397 | chr9:95746061-95753499 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19491 | chr9:95750063-95751459 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22721 | chr9:95750649-95751472 | CD8_primiary |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 95750397 | 95750883 | chr9 | 95749830 | 95750276 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I092987 | chr9 | 95749804 | 95752804 |
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Enhancer Sequence | GGTGCCTCAG TTCTACTCAG TGCAGACTCC AAGGTCCCTC CTCTCTGACT TGAGAGATTC 60 ATGTGCTCCG TTTATCCTTT GACTTGGGGT ATTCTGCACT GGCATGCTTC CAGGGAGTTA 120 CATCCCTTCG CCCCTGATTC TTTCGTGTGG TGGGCTGTCT GCATGCCCAG TGGCCCACCA 180 GCACTTGGGA GGGGCCGTAT GTGTAGTGTG TTTACTGGAG TTGTGAGCAT GCTCACTTGA 240 GCCATTCTTC CTGTACCTGT CAAGTGTTCC TAGACGGTCA TATACCAATT ACACTTCACC 300 ATTTCGCCCC TTAGCGCGCA TGCATGAGTC CATTTATCCA ACTCTTGAGA TCTTATCAGG 360 AAGCTGATTA TCTGTTTCAG GTTTTTCTAT CTATTGGGAG ACTGCATTTC CCTGGTGCTG 420 GCTGCAACCA GTTATTATTT TAAAGAGGCT GTTTAGCAAC CACCTGACCA ATGCAGGATT 480 TTTTGCTCCT TAGTTCAGCT AAAATCCGGG TTCTTGTCTC ATTACCAGGA AAAATTAGGC 540 ACAAGGACAC ATTGAAGGGT GAGGAGGGCG GATTTATTAG ACAAAAAGAA AGCTCTCAGC 600 AAAGAAAGAG GGGTCCTGCC AACAGGCTCC CACCTCACAG ATTGAATACC AGGCCACCAC 660 ACACTAGTTG AAGAGGCCAG GCTTCTCCCC TGCATAAGGC TCCACCCTGC ATAAGGCTCC 720 AAGCTACCAC CATTCCTGGT AGCTCCACCC CATTTCCCCA GTACCTGTGG GCCTCCAGTC 780 CATTGTGGGC ATGCCCAGGC AAGACCCTGC ACAGGTTCCC TTACCTACAC AAAAACATCT 840 GGCATAAATG CTTGTGGGGC AGGCTGGAGA TTCTCCAGGG ACCCTTTCTT ATCTGCCTCC 900 TGCATCTATC AAGACCATCA CCTGATGATG GTCACCTGAT ATTCCTGGTG TGGCGGGGCC 960 CCTGCTCCCC TGCTCATGTC TGCCTGGCTA CCTACCTTAC ACTAATCTGC CATGTTGACT 1020 TCTGATTAAT CATAGTTCCA GGAATGCCTC TAAGATTTCT ATCTTATTAC TGTTCCTTAT 1080 ATAAGAGCAA GTACTTACTG TAAATCTTAA TCTTAGGTCA TGACAACCTT GATGTTACCA 1140 TAAACACATA TTTACCATAA AACCTGCCCT TAGGCTATGA TAAATACAAC ATTCTTGCCT 1200 TTCCCTGAGG GGTTGATTTC AATGTCCTAC ACACTCCTTC TGAAGCACTG TATACCCTTT 1260 CCCTATGGCA TGTAAGTCCT GGGTTTGGGG GTTGACAGCA TGAAGATCTA CCTGTTTTGT 1320 GGCCACCCAA GACCATGCTC TTGTCTGTAA GTTCCCCAAT AAATCACCCT 1370
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