Tag | Content |
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EnhancerAtlas ID | HS007-07693 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr18:45560660-45562440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr18:45562180-45562191 | TTTCTGGGAAG | + | 6.02 | ZNF263 | MA0528.1 | chr18:45560862-45560883 | CCTTCCTCCCAGCCCTCTTCC | - | 6.12 | ZNF263 | MA0528.1 | chr18:45560892-45560913 | TCCTCCTCCCAGCACTCCTCC | - | 6.85 | ZNF263 | MA0528.1 | chr18:45560880-45560901 | TCCTCCCAGCCCTCCTCCTCC | - | 6.98 | ZNF263 | MA0528.1 | chr18:45560877-45560898 | TCTTCCTCCCAGCCCTCCTCC | - | 8.1 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26544 | chr18:45559340-45565498 | Esophagus | SE_34739 | chr18:45561883-45563967 | HeLa |
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| Number: 2 | ID | Chromosome | Start | End |
GH18I048033 | chr18 | 45559615 | 45561470 | GH18I048035 | chr18 | 45562050 | 45564036 |
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Enhancer Sequence | CCACACTCTG GGCAACTCTG CATCTTTGAA CACCTGCAGG TATGAACTGG ACTGCCGGTC 60 CCCCAGTGCA CAGCCCACCA CATTACAGGG TGGATGCCCT GTAAACCCTG GCTCCTTCCC 120 CGTGTGTGCA TGTCTTGTGC TTGGACACTG ATGCTCTATC CTTAGGGCCC TCCCAGAAGG 180 CCAAGCCCAG AGCCAGGGTG CCCCTTCCTC CCAGCCCTCT TCCTCCCAGC CCTCCTCCTC 240 CCAGCACTCC TCCCTGCACG TGGCATGGAG TTCTGGTACC TGCTTTGATG AGAACCTGTG 300 GGATGCTCTT TCGTACTCTG CACAACACAC AACACTGAAT GTAGATAGAG AGGAGGCTCA 360 CTGCGCGTTT GGTGACTGAC TAGTGGTGCC AATTTCAGAA CTCTCCGACT ACAAATCCAA 420 CATGCTCCCC TCTGGCCCTG GTCCCCTTGT CTGCCATCTC GTTCCATCTC TCTGCATCAG 480 GGACAGCCAA GGACATATGC ACCCAAGCCT CGGTCTACAT GCCTCCTTTC AGCCTGGAGA 540 GCTCATCGTC GGGAAAGTCA TGTGAGTCCT CATGAGCTCA TTCCCAGAAT CAAAGAAAAG 600 GGCTGTGGGG CCTTGGCCTG AGGTCTGTGG CCTCCAGAAA GGCTCCCAAT CAGGATAATG 660 CTTTCCCAGC AGCCTCTACC TGGACTTCTT GTAACCCGAT GGTTTGAGAC ACACTCTTCC 720 TGCTACCACT GCTAATGCCA TTACATTATC TTAATAGGGT TCCCAGAGCT GCCAGGAGTG 780 GGAGGACTAC AAAGAAAATA GAGGGAAGAC AAAAGCCAGG CTGCTGGCTT ATCTGGAGAG 840 CAGGCAGCTG TGGGGGCACA AAGGTGGTCA GCATTCGGCT GGCACTGGAG GAGGCAGGTG 900 GAGACTAAAA GGCACAGCCT TCGGGGTTCA GCGGAACTGG AAAGCGTGCC TTGTCAGAGA 960 GTGACTGCGG TGCAGAGGTC GTCCATCCCC ACCCAGGACG GTGTGCTCTA TGGGACCTCT 1020 GCTGTCTCTG GGCCAGTCTG TTTTCATTTT GCAGTTTCTT GCCTTCACTA CTGTCCCCAT 1080 CAGGCATGGC TGGGGCATCT CTGGGAGCCA GGCTGTGACA GGATGCAGGG GCTCCAGGAG 1140 GGAGACCAGC CAGCCATGCT CTCTAGGAGC TACTAACAGA AGGGCTGGGG GAGGCAAGGG 1200 GCAAGTCTCT ATGGCCTGCA ATCAAGGACC CATGTGGTGG GAATTAAGAG GCGGAAGATG 1260 CACAGGCTTT CACAGGGCCC AGGGCCAGGC CCAGTTGGCA GTGATGGCTG CAGATGGGGC 1320 AAAAAGGTGT GCGGGGGCCA CCTGGACCTG GGATGTCCGT GGGCAGGGAA AATACCCACC 1380 AAGCATAGCA GTGTCCCTGT GCATGAAGAC AAATGCTTTA TCTTCCTGAG ATCACATGCT 1440 CCCTGTTCTT CTAGGCCCTT CCTAGGCATC ACCTCTGGCC GAAGCCTGCC ATCCTAACCT 1500 TTGGCTCCTG GCTTCCAGAC TTTCTGGGAA GAGAAGGGAA AGGATTCCTG ATGAAGAGGA 1560 TCTAAGGTAA TCTTGGTCCA GACTGCCTCT GCCCTATGAC CTGGAGCTGT TTCTGTGTCC 1620 CAAGTCAGAC CTGAAAGGGA CAGGAGCTGC CTCTGTGGCC AGCACAGGCA CAAGCCTTTC 1680 CCAGGAGGAA AACGGTGTCT TTGAACTAAA CCGAGGGAGT GCACAGGCAA AGGGAGCCCA 1740 AGTGGCTATG GGGTGACCAG AGCTAGGAAG GGACAGCATG 1780
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