Tag | Content |
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EnhancerAtlas ID | HS040-20089 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr2:73334050-73335190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr2:73334872-73334883 | AGCCACACCCT | + | 6.02 | MYB | MA0100.3 | chr2:73335057-73335067 | ACCAACTGTC | + | 6.02 | ZBTB18 | MA0698.1 | chr2:73334441-73334454 | GAACATCTGGACA | - | 6.09 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53911 | chr2:73331600-73341080 | Spleen |
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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 |
GH02I073106 | chr2 | 73333368 | 73336028 |
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Enhancer Sequence | GGAGGTGCTG GCTGCCCCTG GGAGCCCCGT TTTGGGAGGC CCCACTTACT GCTCCTGAGA 60 GGCCGGGGCC CAGCTCCATA CAGAGGCCTC ATGTGGCCAG CCAAGTCCCT CTCCTCTCTG 120 GCCACCATTG TTCCCAAGGT AGAAATAACC TCAGGCCAGC TCAGTAAGGG CACTGTGATC 180 AGACTCTTCC CTGAAGGGAC TGCCAGGTGC ACAGCAGACT CACATGTGGA CTCATTTTTA 240 TTACTTGGCT GTGGGGAAGA ACAAAACTGC TTCATGGCTA CACTATTTTG CAAAGGAAAG 300 AAAAAGAGGA CTGCTTCCCC TGGAGCAGAG CCACAACAGC TTCTGTTCTT GTATTCATCA 360 TCTGTCCCTG CGTAGGGTGA GAAGGGCAGG AGAACATCTG GACAAGGCCA GGCCAGTGGT 420 TTAGACAAGA GCGTCACAGC ACTGAGGTGG CAGCAGTGAC AAGTGGGGCG GGCAGCTCCC 480 AGCAGAGAAG GACAGCCCTC AAGGTCACCG GGATGTGGCT CTGCTGAGCT GTGCCTTGCA 540 GCCAGCTGCC TACAAGGAGA GACAGGTGGG GCAGAGATGG GGCTGACCAC AGGCCCCTTG 600 AAACTCCCTG GTCCCAGCCA GGGCTCAGGG CCAGGGGCAG ATGGGGAGGG CAGGGGAAGC 660 TGCCAGGCCA GAGAGGAGGA GCTGCCCAGC CTGACTGAGG AGTCACACTT CCTACCCCGC 720 CCCACACCCC AAGACGCTGC TGCTCAAGCA ACCCCAAATA AAAACCACCC CATAACTAAG 780 GGCCGTGGAG CCTCGGCATA CCAACGACTG GCTTCTGAGT GCAGCCACAC CCTTCCTCTG 840 CAGCCAGAGT AGACCTCCCC AGCAGTGCCA CAGGCCTCCC ATGCCAGCTC TGGGGCCGAG 900 CAGGAGCCAA GGCCAGGGGC TCAAGTGACC ACAGCTGTTT CCCGAGGGGC AGAGTCACAC 960 CCAGAAGCCA ACAGAGAGAA GGCTGTGGGG TCACGCACCA TCTGCCCACC AACTGTCTGC 1020 CCAGGCTGTC TGTGGGCTAC GGGATAGATG GAAGCCCTCA AAGACCATCC CAGCCTTAGG 1080 CTAATGGGAT GCATGTCCCC TCAGGTGCCT CCCAGTGCCC CCAAACCCAC CCACCTAAGG 1140
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