Tag | Content |
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EnhancerAtlas ID | HS101-02258 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:110178550-110179820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:110179171-110179182 | GGATGACTCAG | + | 6.32 | JUNB | MA0490.1 | chr1:110179171-110179182 | GGATGACTCAG | + | 6.14 | NFE2L1 | MA0089.2 | chr1:110179171-110179186 | GGATGACTCAGCTAA | + | 6.49 | Nfe2l2 | MA0150.2 | chr1:110179169-110179184 | CAGGATGACTCAGCT | + | 6.44 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_04689 | chr1:110178416-110180011 | Brain_Anterior_Caudate |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 110179668 | 110179765 | chr1 | 110178759 | 110179342 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I109635 | chr1 | 110178587 | 110179578 |
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Enhancer Sequence | TTATATTTAA TGAGGGGGTG TGGGTGCATT TTAAATGCAA GTGAGTGTGG GGCCTCCAAG 60 AATCAGATGC AGGGTCTATA AAGGACTTAC TTAAAATGGC TCAGCCCCGC AGTCCCACTC 120 TGGGCCAGGG GGGTTGGCTC AGATTTTGGT CTTGCCGTCA CCTTCAACTC TCCTGCCTCC 180 CTAAATAGTC TGGGCAGATT TGGAGCAGCT ACTGCTGCCA CTGGCATCTT CTCTGAATCT 240 GTGCAACAGA TATGCACAGC TGGAATTTCT GTCTCCCCTT TGCAGATGAG AGACTGACCT 300 GGGTTTAAAC CTGAGTGTTC TGTTTATTAG CTGGGCAAGT CAGCCCTCCT CCCTGACTTC 360 CCAGGCCTGG AGGAGATATG CAAAGGGGAG TGGCTACCAA TCCATTCCCA CCAGGGTCCC 420 AAGCTACTGC TGGGGTATGC TGGTGTGTCT ACTACGCATT TGCCATGGTG GGGTAAAATA 480 CCTATGAGCA CCTGGCATTG GGCTGAACTC TTTGTAAGTG TGAATGTACT TCCAGCTCCT 540 AGAACTCTGC ATGATATCTA TCACCATATT CCCTCGCGTC AACAGGGAGA ATGAGGTTCG 600 GGAGGTTATG TAACTTATCC AGGATGACTC AGCTAATGAG TGCCAGAGCT GGGATTTGAC 660 CCCAGAACTG TCAGGCTGCA AAGTCTTTGT TCCTCCTACT CTATCATGGT CCCTGGGGTA 720 CGTGTCTGGT TGAGGGGGTC CCTCTAGGGG TGGGGTGCTC AGGGAAGGGA CAGGGTCAGG 780 CTCTGATGAG CAGAAGGATC AGTGCGGGTG AGTCTAGAGG CAGAAGGGTC ATGGAGGAGG 840 CTCCTGCCAC ATCCCGGGTG TGATTGACAA GGACCTGGCT GGTGGCAGTG TGGGTGGAGA 900 GGAGCTTTTG TGGGGAGGCT GCTAAGACCA GTAGTTAAGA CAGAGGTGGC AGAGGTGGCC 960 ACAGGATTGT GATTGGCTGG CACAGCCTGA TATGAGATCG AGAATGTGAA TGCTCTGAGG 1020 CGGCTATTAG CCTGACCCCT CCCGGTTACC TTATACCCAT CCCAGTCCAT ACACTGCCAG 1080 AGAGGTACTG GGTTTGTGAT CCCCGGGCTC TATCCCACGG CACAGCTGTC ACTTATTAGC 1140 CATAAGATCC TGAAAATTTC TAGGAACTCT GAGCTTTAGT TCTCTGATCT ATCAAATGAG 1200 GATATCGGGG TCCACGTGTA TTGGTTTGCT ATGGAGATTA AATGCTGTTT ATAAGGCAGA 1260 GTTCAACGAC 1270
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