Tag | Content |
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EnhancerAtlas ID | HS108-12220 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:69168350-69170770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr14:69168841-69168856 | GGGGTCAAGGCCACC | + | 6.05 | TBX21 | MA0690.1 | chr14:69169043-69169053 | TTCACACCTT | - | 6.02 | TFAP2A | MA0003.3 | chr14:69169018-69169029 | TGCCTGAGGCA | - | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_09837 | chr14:69169371-69170748 | CD14 | SE_26618 | chr14:69169542-69174185 | Esophagus | SE_36049 | chr14:69169327-69170950 | HMEC | SE_55866 | chr14:69168951-69172331 | u87 | SE_65119 | chr14:69169223-69170772 | NHEK | SE_67722 | chr14:69168951-69172331 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I068702 | chr14 | 69168876 | 69170570 |
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Enhancer Sequence | TGAGTCAATA TATGTATAAA TAAATACATG TACTTAAACA TAAACTTACT ATAAATGAAT 60 ATAATAGAGA CCCAATAAAC TTGGGTTGTT ATCATTTTTT TTTTTTAAGA CAAAGTCTCA 120 CTCTATCGCC CAGGCTGGAG TGCAGTGGCG CGAACTTGGC TCTGCCTCCC GGGTTCACGC 180 AATTCTCCTG CCTCAGCCTC CTGAGTAGCT GGGACTACAG GCACCTGCCA CCACGCCTGG 240 CTAATTTTTT GTATTTTTAG TAGAGACGGG GTTTCACTGT GTTAGCCAGG ATGGTCTCCA 300 TCTCCTGACC TCATGATCTG TCCGCCTTGG CCTCCCAAAG TGCTGGGATT ACAAGGGTGA 360 GCCACTGCGC CCAGCCGGGT TGTTATCATT ATTTAAGGAT TGAGACCCCT TTTGATGTTT 420 GCTGCTGTCA AGAAAATATG TGAGCACAGC TTCTTCCCCC ACTTTGTTAC CGCCCCACAC 480 ACACTCAGGC AGGGGTCAAG GCCACCTGAG CAGCTAGATG CAGCCACTGA GGCCCCAGCC 540 CCCATTGTAG AGCTGCTGCT TCTAGGAGCC ACATGCCAGG GAGCAAGCAG CAGTCAGCAC 600 TGGAAACAGG CTACCCCAGC CTCAGTCTCC GTGGGTACCA CTCAGGTGCC CAGCACTGCG 660 GGAATCCCTG CCTGAGGCAG CCTGGGCTGG GAGTTCACAC CTTGATGCCC CAGGGTCCTT 720 GGATAGTGAT GTGTCAGTAA CACTTCAAGC AACCAGACGA GCTGCTCTGC AGGGAAGAAG 780 CCCACTTGCA AGGGAGCTGG ACATTCCCCC AGCCCTGGGA AACACAGTCC TGCTTGCTCT 840 TGAGGTTGGG TCCCCATGAG AAGGGGGTCA AGAAAGGACC AAGAGCATCA CGGGTTTTTT 900 CTAGAGCAGA GGAGAGCCCT TAAAGCAAAG AGACTATCTG TACACGAGAG CCACTGAAGT 960 GCAGAAGGAA GGCCAGGGGA GGGGCATGGA GGCAGAGACA GGGGTTCAAG CCCCAGCTCC 1020 CCTTCACTGT GTGAGTTATT TAATTTCCTG AGCTTTAGGC TCCTCCTCTC TCCTAAGAGG 1080 ATAGCGCCAC CTCCCTTAAG GGGTACCTGT GGCTGTATGG AGCAATGGGA GAGCAAAGAG 1140 GAAACCCTGG TGCATCCAGC CTTCCTTCAG AGACGGAAGC CACAGGCCCA GCCAGGAGAT 1200 CTACCCAGGG TGGACCAGCA CATTTCTGGG AGTCCAAGTC AATGCAGACA GAGGGCTCTC 1260 TAGGGAACAA AGAACTGAGA AGAGGAAAAC CACCTCTGGC TCTTGGTGAG CCTGCCAACC 1320 TCCTGCAGCC CCTCATAGCC CAGGACCCCT GGAGGTGAGC CTGACTCTCA GCCCTGGCAC 1380 TGGAGAAACT CACTCTTCCT TGCCCTATTG GTCCCCATTT CCTTTTTCCT TGGGCCCCTC 1440 TTCTTCTAGC CTGGGCAGAG CTGAGGAGGA CAGTGGGGGT TCAGGCCGCC GCCAGGCTGG 1500 GGAGCTCCCT GCAGGGCTGG GAGAATAGGA TGGACAGCGT TTTGCCAGAG CCTCATGGGA 1560 AGCTTCCTTT CAGGCAGCTG AACCCATTTC AGGGGTAGGG AGCACTGATC AGGGGTTGGG 1620 ACATTGCCCC GGGAGGAGGA TGAGGATGTT TCCAGGCCTC GGCTGACTCA TGGTAGTGAG 1680 TATTAGTCAC TCCCTCACAA GAATCAGCCC ACATCCTCTA GTAGCCTCTT GTCTCCCAGA 1740 GGCCCCTGCC CCATGTTTAC CTGCCTGAAG CTCCTCTCCC GGCCGCCCCC ACCCACATCC 1800 GCACAGTTTG GGCAGACACA AGAGCCCCGC ATCACTTTTC ACTCGAGGCT CCTCTGAGAC 1860 ATCAGCTTCC TGCAGGAGAA ATCTTCAGGG GGTTTCTCTT ACAGATTTGG GGGTCAAAGA 1920 CTGGGTTCCA ATCGCAGCAC TGCTGCCTTG TATCTCTGCT TCCTGGGCAA ATTATGTCAC 1980 CAATCCGGAC TGTTGGGGAT ATTTTCCCCG AAGAGTAATA ATAATATTAT CTAGTAGGAT 2040 TGTTGTGACA ATGAAATCAT ATAAAGTGTG AAAGTTCCTG GCACAAAATA AGTGATCGAT 2100 GCATGGTAAT GAACACTATT ATTATACATC AATAAAAGAA AAAAGGTCCC TTATATATAG 2160 CATTTTAAAA ATAAGGTAAC AAAACCCTTG GCCCCTTGGC CCTGTGAAAC TGTGGGCTGA 2220 CATGGAACAA AATAAAAGCA AGTAGAGGGC CAGGTGTGCT GCCTCACACC TGTAATCCCA 2280 GCATTTTGGG AGGCTGAGGT GGGAGGATCA TTGGAGTTGA GGAGTTGGAG ACCAGCCCAG 2340 GCAACATAGC AAGACTCTGT CTCTGCAAAC AATTAAAAAC TGAGCTTGGT GTGGTGGTGC 2400 ACACCTGCGT CTGTGGTCCC 2420
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