Tag | Content |
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EnhancerAtlas ID | HS094-07882 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr11:102112740-102114180 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr11:102114071-102114083 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr11:102114071-102114083 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr11:102114069-102114084 | CTACTAAAAATAGAA | + | 6.57 | Myod1 | MA0499.1 | chr11:102113096-102113109 | TCCAGCTGTTCCT | + | 6.09 | Nkx3-2 | MA0122.3 | chr11:102113688-102113701 | AAAACCACTTATT | + | 6.14 | TBX20 | MA0689.1 | chr11:102113044-102113055 | CTTCACACCTT | - | 6.32 | TBX21 | MA0690.1 | chr11:102113045-102113055 | TTCACACCTT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_00051 | chr11:102104808-102114317 | Adipose_Nuclei |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I102242 | chr11 | 102112984 | 102113885 |
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Enhancer Sequence | ATAAATAAAA TAAATAAATA AATAAATCAA GCAAAATAGA AGAAACCAAA ACATGCAACC 60 ATCCCAAATA CAAATACAAA ACATGGATTT AAATGATTTG TCACGTCGCT ATTTTTAAAT 120 GCAGGGCGAA TCCCATTAGA ACCTTTCTCT CTGTGGATAA AATACAAATC CCTGCCTAAT 180 AAGCACAATA AGAGAATGTT GGCAATTCTG TTATTTCATC TCTAGCACGA ATTGACCTCA 240 TTTCTCCAAC TGGCTTTGTG CTTTGAAAAA CTGACCAAAA TGCCACGCGT GTGTTTGATT 300 AGCACTTCAC ACCTTGTTTA CAGTGCACTA GAGAAACTGG CTGTTGTTGG CATCCGTCCA 360 GCTGTTCCTG ATGAGTTGCC AGGCTGAGAA ATCTCCCTGG ATTGGGATAA CTGGAACAAA 420 GGCCAGGCTG ACTGAAAAGT CAGCTGAGGC TGGGCCTGGT GGCTCACGCC TGTAATCCCA 480 GCACTTTGGG AGGCCGAGGT GGGTGGATCG CTTGAGCCCA GGAGTTCAAG ACCAGCCTGG 540 GCAATACAGT GAGACCTCGT CTCTACAAAA AATAAAAAAT GTAGTCAGGC GTGGTGGCAC 600 ATGCCTATAG TCCCAGCTAC TCAGGAGGCT GAGCCAGGAG GATTGCTTGA GCCCGGAAGG 660 CAGAGGTTGC AGTGAGCCAA GATGGTGCCA CTGCACTCCA GCCTGGGTGA CAGTGATACT 720 GTCTCAAAAA AAAAAAAAAA AGAAAAAGGA ACGTTCAGAT GGTCTTTTTT ATTTTTGGTG 780 GGGTGTGGGG AGAGATGCCC CAAAGCCTGA GCTAGACTCC TAGAGCTCTT TAATCCCCAG 840 AACCAGCATC TATGAAAGAG GAGACTTTTT ACAGCCCTAC CCTCTTTTTC TTTGGCTACT 900 GTGAAGTGTT TTCCCTCTGA GCTAAGGTAT AAATGGCAAC TGGTTTCCAA AACCACTTAT 960 TCACATAGCT AGTGAACCAT TTGGGCTGGT ACTGATAGCC TCCCCTGAAC CATCCCAGGC 1020 ATGGGGAGGG TTACAAGTGC TTCATGATAT TTGTAGGTCA AGACCCTTGA CACCCTGCCC 1080 AGGGCAGCCT GAGCAGGGTA GTTGGGAGTG ACCCCATATG GTCAGGACTC GGGAGCCGGA 1140 TCCCTCAGGA TCACAAAAGC ACACAAGGAG GTGTGAGGCA GAGTTCAGCC AGGTCTCGAA 1200 ATGAGAGAAT TGCAGGCCAG GCACGGTGGC TCACGCCTGT AATTCCAGCA CTTTGGGAGG 1260 CCAGGGCAGG CAGATCACTT GAGACCAGAA GTTCAAGACC AGCCTGGCCA ACATGATGAA 1320 ACCCCGTCTC TACTAAAAAT AGAAAAAATT AGCCGGGCTT GGTGGCGGAC GCCTATAATC 1380 CCAGCTACTC GGGAGGCTGA GGCAGGAGAA TTGCTTGAAC TTGGGAGACA GAGGTTGCAG 1440
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