Tag | Content |
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EnhancerAtlas ID | HS197-17398 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr5:134491950-134493430 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr5:134492399-134492410 | GGGCGGGAAGA | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26601 | chr5:134488649-134494073 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I135155 | chr5 | 134491368 | 134493460 |
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Enhancer Sequence | AAATAACTCA GAATCATGGT GATCTAGGGA GTGAAGTATC CTGTGCATCA TATATTTTTC 60 CTTGGGTTCT AACAGCTTTC CTTGGGGCCT AGCATGAAGT GATTTTGGTG GTTCCTCATC 120 ATGCCTGCAA TTGTGTGGTC TTTTCCGCCT GAGGGTTGCC ACAGTGTAGC TGCCCTCTAT 180 CCTGAGGTGC CCAGGGACTA GTGAAGGACA GGAATCGGGA CAGGGCCCCT TGGGTCCCAC 240 TGCACAGATT CCCATGTGCT CACTGCTCCC CAGCCCTTCC TGGAGGCAGG CGTGGGATGG 300 GTCTGGAGGG AACAAGGACA GCTAAGTCAT TGCCATGGAT TTAACCGGCT GGCTGGGCCC 360 ATATATGCAC AGATTGTGGG GATGTGGACT CCTCCTTCCC ATGCTGGAAA TGGGCCCCAG 420 AAAGCTACCA CCTGCCACTT CTGTTGGGCG GGCGGGAAGA AGCTTGCACC ATAGATACTG 480 TGAAGTCTGC AGGTTTCACT CGGTTGGGAT TTGTCATCTG GCAAACAGTC AAGTATCTGC 540 CATACCTGGC CGAGTCAGCT GCAGCCTTCA TGGCCAATCC GCATGATGAA GTATCCAGTC 600 AAGTTTTGGC AATTCCAAAG GTGTGGCAAT CTTGGTTGCA AGGGGCCAGT GGGGAGCATT 660 GCGACAGAGG CCCTTGTGCT GGACCTGCAG GACGCCCCAG GAAGAAGGTG GAGGGTGGAG 720 GGCACCCTTG ACAGTTGACA TCTGTGTCAA CAGCGCCCAG TGACACACCG GGGGAGGACG 780 AGCCTGCACT TGGCAGGCCA ACAATGAGCT GATTGATGCA ATGAACTTTC CCCTCAAAGG 840 CCCCACCACT GCCTGGGGAG CCTGGGCCAA TGGTGGTCTG CCTGCTTCCC CTGTAGCGAT 900 CCGCTGGCAG CCTCAGAGCA GGGAATGGGG GTGGGTATTG GCTCCTGATG GGGTCAAGAC 960 TTGTCCAGGA TCCTCTAGGA GCCTGCTGTG GAGTAAGGAG AAGGCTGGCA GCTCCTGGAC 1020 ATGCAGGAAC AAAGGCCTGG GAGAAATGAG TGGTGTATGA GTGGGAGTGG CTGGGCCCTG 1080 GGTGGGTGAT GTGTCTACGG TGCCTCCCAC CTGGCATGAG GAGGGAGGAG CTTCATGAGC 1140 TGCTGGGGAG GCAGGTATGT TTGTCCTCCC ATAAAATGTG GCCCAATTTA TAGGGGTTGC 1200 AAATGTTCCC TAGAAACCTT ACCCATACTG CACGTCTGGG CTCAGTTCAG CACTGGGGAT 1260 GAAAACCTTG GCCCTTCTTC TTAGACCCTG TCCCTCCTTC TCCATGTATA CATGCATGTG 1320 TGTGCGCACA CACACGCTCT ACCTTGCCAG CTGAGGTTGT ATGATTCATG TTGCTGGGGA 1380 GCTCAGACTA CTCAAGGCCA TGGTGCTGGG AGACTCCATA TCTGGGTACG GATATTTAGT 1440 CTAAGCAGGC CTCAGGTCAT GGGACCCTCT AGTTGACTCT 1480
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