Tag | Content |
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EnhancerAtlas ID | HS092-01798 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:59062210-59064010 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr1:59062649-59062664 | ATTGCTGAGTCACAC | - | 6.91 | NR3C1 | MA0113.3 | chr1:59063620-59063637 | TAGAACAGAGTGTTCCA | + | 6.18 | NR3C1 | MA0113.3 | chr1:59063620-59063637 | TAGAACAGAGTGTTCCA | - | 6 | NR3C2 | MA0727.1 | chr1:59063620-59063637 | TAGAACAGAGTGTTCCA | - | 6.04 | NR3C2 | MA0727.1 | chr1:59063620-59063637 | TAGAACAGAGTGTTCCA | + | 6.22 | Nfe2l2 | MA0150.2 | chr1:59062651-59062666 | TGCTGAGTCACACAT | - | 6.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26866 | chr1:59062067-59063099 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I058596 | chr1 | 59062068 | 59063099 |
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Enhancer Sequence | CTGTGACTAC AGGCATGAGC CACTGTGCTC AGATGATTTA CTGTTAATGT TTCTTTTTTA 60 TGTGACCTTT CAAACTTTAG TTTTATTAAT CATGGTAACG TATTTTGGGA GAAAGCTGTG 120 ACCCTAGACA ACAGGTGTCA AAACCAAGCC CCATAGCAGT GGTTTTCCCT TGATCAGCCC 180 CAGTTGCTCC CTCTGGCTTC ACTTCCTCCT GGCTGCCTCT GAACTCACCG TGCTAACACT 240 TCCAACTGTA GTCAGGTCAC TGGGGCAAAA TGCAGAGGAA CTGGATATCG CAAAATGCAG 300 AGGAGCTGGG TATCCCAAAA TGAGTTCTGC ATCTGTTTGA GATAAGACCT TCATTCCTCC 360 AATGTCACTG GTATGTCTGC TTAGAGGAAA GGAGCTCCTG ACTGGCTGAT TTTACCACCA 420 ATTTTGCCAG AGCCTAGGCA TTGCTGAGTC ACACATGTAC CTGCTCTTCA GGCTCTTTCT 480 TCTGAAAAGT AAAACTCTTC AGTATCGTGG CTAGGCTTCC ATACAGACCC AGCCTTCACA 540 AACAAACAAG CTGTCAGGTC AAATCCTTGG AGAAGTGAGT CTGTATTCAA ACCAGAGCCC 600 TCCAAGGGCT GCATGGGAAA TGTTCCCTCT CTGGGATTCA GTCTGTTCTG AGGACTGGGC 660 AGCGGGCAAC CTCTGAACAA AGACAATTCC TGTATTTTGA GGCTCTTGAG CATCGCGTTG 720 ATCTTACGAA GTGGCCAGGC ACGCGCCAGC CTCCTCAGAG GCAAATACTC CAGGGAACAA 780 CGTTGCTTAT TGACAACAGA CGCCTGTGAG TGGGAAGCAT CATTCCCTTC CGAGAATTTG 840 ATTCCATTCA AGGCTGCTGA AGAAAATTTG TTTTTTAAAA CATGACAGAT TTTTTCCAGA 900 TGATATCCAG GTTTGCTAGC AATTTAAGAG ACCTGCTATA TTTTATACTG AGTGTATCCA 960 CTCCCTGCAA AAAACAGATC ACAGAGATTG CAACCCTCCC CATGTTGAAA GAACTTTTCT 1020 CCAACTGATG TCATTATCGC CTTATTTCAA GCTGTTCCCA CAGAATTCAC CCTGATCTTC 1080 TCCTTTGTGC CTTCATTTAT TTATACATTC AACACATGCT TTCATTTCAC ATGAAGAGAT 1140 TGTCACATTC CAGGCACTGG GCAAGCTATT GAGAATACTG GGGTGTACAA GATAGATACA 1200 CTTCCTGCCA TGATGGAGTT TAGCAGGGAG GGCTGACCAG TTCTTAGAGG GTGGTGAGTA 1260 TAATCACAGG GCAATATGGT GGGTATTCTC AGCAGGTACT GGGGATGAGG TGGGGCATCT 1320 AGACAGGCTG TGAGGCAGGG AACATCTTCT TAAGCAAGTG GAGTGTAACC CAAGACCTAA 1380 GGATGAGTAG TACTGGGCCA GGGGAAGAGG TAGAACAGAG TGTTCCAGGC TATGCAGATG 1440 TCGTCCACTG GCACTCAATA TCTACTCCAA CCTTCTTCTA CCGTGTTAGT CTGGAAAGCT 1500 AAAAGCCACA TTTTCTGGGT TTCTTTGTAG TACGTGTTCT GAATGTGAAT TAGCTCCATC 1560 AGTCAGTGCA TTCCTGCGGG ATTTGGAAGA TGGGGGTGCT GCAGTGGCCT CACCTCCCTG 1620 CTTCTGTGGC TTCTGCTGGT TGGTAAGCTC CTCATGGACG GAAGTCTGGC CGCCACAAGG 1680 CACTTCTTGA TTTTGGTGGC TTCCTGGGTA TTTCAGTTTC TAGGTTGTGG CTGTTTGCTG 1740 GTTTTGGTGG GTTTTTGATC CTGGCAGAGA GCTGCTGCAG GGGCAGCTTC CCAATTTGGC 1800
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