Tag | Content |
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EnhancerAtlas ID | HS007-07696 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr18:45598700-45600430 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr18:45599768-45599779 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr18:45599768-45599779 | CTGAGTCACCC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26544 | chr18:45598310-45605257 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I048072 | chr18 | 45598970 | 45600373 |
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Enhancer Sequence | AATGAGATAA TGTATATGAA GCCTGGCGCT CAGGGCCAGG AGACTCCTCC GATCTCTCAC 60 CCTTTCCCCC TTCTCCCTGG GTGGCTGCAT CCATTGGCCA GGTTGGCCTC AGGCGCCAAC 120 CCCAGCTCAC CTTTCCCAGG TCGATCTGCA GCCTCCTTCC CATGTCCCAC TCCTGAAGGA 180 GGGCCGCCAG CTTCCTGCGA CTCAACAGAC AGACACAGGG GCAGGAGGCC AAGCTTCACA 240 GTGTCTCCCC GGGGCGCTTG CAACAAGCAA ACAAGCAAAG ACTGAAATAG GGAAGGTAGA 300 GTTTCACACT CTGTGGGAAG TTTGTGGCAG AGATATTTTT AGGAGGGGAG AAGGTGGGAG 360 ATATTTTTAG GATGGGATGC TTTTCCCATT GCTCCTCCAA TCCCACCTCC CTGTGGGGAA 420 CCGAGGAAAG GTAGCATTAA GAGCCGCCTG TGATGAAGGA GGCAGCCGGC ACTGCTGGGG 480 AGAAGGCAGC CGCTCTCCGC TTCATCCTTG GGCTGGGACC CCAGATGTTT GACCCTGGCC 540 AGCCCCTTGC TGGCCTTCCC GACAGAGCCA CTTCCCTTTT GGGAGTGCAG CCTGGAGTTC 600 CCTTCCCCCT CCAGGCCACA GCCCCACTCT CCCTTAGGAT GACCTGAAAG GGAAGTTTAT 660 AAGAGGAAAA GGAATGAACG GGATCCTATT TAACAGCACA TGCTGGGCGG AGGAACTTCC 720 TGACAGGAAC CAATGTGGAA ACCAGGCCCA GTTTGGCCAT GGAAAACTGG TTTGGCTCAG 780 AACTGGCCAG AGTGGAGAGG AGACCTTGGG CAGCTGCACG TCGCAATTAA ACTGGACTTG 840 TCCGACTTCG CTTTCTTTCT TGTCCCCTCT AAGCAAGCAG ACACTATAAT AATCTGCACA 900 CCACAGGGGG TGTGCAGATT ATTTTTTTAA GTCTAGGGGA AAGAAACCCC ACCCTCATTT 960 AGGTCACAGA GACATAAAGG GCTACTGGCT AGGCTCAGCA AATCAGGAAC AGATGTAGGC 1020 AGCGGAGCAG GGCCAGGCGA GCAGAGCCGC TGCCACCAGG CGCCCAGCCT GAGTCACCCT 1080 GGCGGGGAGG GCGGGAGGTG GTGGGCAGGG GTGGCCGTCT TTATTTGTGG GCTTGGGTGT 1140 GGGGTGCAGG AAACAATGCA AACAGAAGAG TCCCCGGGGC TGGGACAGGC GCAGGGGTGC 1200 GGGCAGGTAC GGACAGGCTC CCAGTGGCTG CTCTTCTGGG CCAAAGGATT AAAACAGGCC 1260 CTGAGTTTGA ACAGGGAGAA GGCTCTGCTC CTCCCTCAGC CTCTTTCTCT CCTTCCCCTG 1320 CCCTCCCTCT CCCCCCACCC AAGAAGACCT TATTTCCAGG GCTGAGTCTG GCTGTGGCTG 1380 GCCGGCTGGC CTCCGCCCTG GCTCCCCAAC CCCTCTCTTT AAGGGCCAGG CTGTCCTGTG 1440 GCTGGCAGCT GGCAGGAGAG GCCTGGGGTG GACGTTTCAG CCCTTGCTCC CCGAGTTTCT 1500 GCACAAAGCC CTATCCTCTC TCCTCAGTTC TCCCTTTTCT CTCCTCACTC TGATTTGTCT 1560 CCTGTAGACC CCCAAAGAAA TATTAGCTTC TCAGGGCAAA GGCCCTGTCC CTGCCCCTCA 1620 GGCCCCAGCC AGGCCTGCAG TGGGTATTCA GTCCTCATTA TGACTTTCTC GAAAAGAAAA 1680 ATTTCTTTTT TTTTTTTTTT TTCAGACGGA GTCTCGTTCT GTCACCCAGG 1730
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