Tag | Content |
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EnhancerAtlas ID | HS117-02297 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr14:75405920-75407350 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr14:75406896-75406907 | AACAGCTGCAG | + | 6.02 | SOX10 | MA0442.2 | chr14:75406321-75406332 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr14:75406322-75406332 | CCTTTGTTTT | + | 6.02 | TCF7L2 | MA0523.1 | chr14:75407239-75407253 | TAACATCAAAGACA | + | 6.01 | Tcf12 | MA0521.1 | chr14:75406896-75406907 | AACAGCTGCAG | + | 6.62 | ZNF263 | MA0528.1 | chr14:75406177-75406198 | CTCCCTCTCTCTTCCTTCCCC | - | 6.08 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38122 | chr14:75405657-75410020 | HUVEC |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I074938 | chr14 | 75405505 | 75410103 |
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Enhancer Sequence | CACAGCTGCA GGCCTCCCTC TTGGGAGGAC ATGGACAAGA CAGCTCAAGG ACATGCACCT 60 TCCGCCATGT CCACCTGACC CATGGGCAAC GACTGCTGGG TGCCCCAAGG AGTCCCTGCC 120 CTGTCTGTCT CTGCCTCTTC AATCCTGCCC TCCCCCAACC TCCCTGTCCA GATGGCGCGT 180 GGGCTGATCT CAACAGCAAA TCCAGATCCA GGGAGAGGAG GGGAGGGAGT CAGCACCCCA 240 GGACTCCAGT GACCCATCTC CCTCTCTCTT CCTTCCCCTG TCCTGGTCTT CTGCTTATGG 300 AGACTGAGGA AGGGGGTGCT GGGAGATTTG GGGGCATAGC AGAATTGCTT TAACCATCTC 360 TTAATAAATC CTGTAGGCAA ATGGGCCTAG TCTCAAATGG TTCCTTTGTT TTAGAATATG 420 GGGTACTCAA GGCCCTTTTT CCTTAGCTCT GAGTCCGGCC ACCCATTCGA GCAGCAGAAA 480 AGGCCCACCC AGTACCCTCT GGCACTAGAG CATGGGCTGT CTCTCCCCTC GCATGTGTGG 540 TCCACGAGAG CAGGGTCCTG TGTGTCTGTC CCCACTGGAT CCTGGATGCC TAGTCAGTGT 600 CTAGGACACA GAGGGTGCTC CACAAATAGA TGACAAGCAA ATCCCTCTAG GACCTAAATG 660 GCTGGAACGG CTGCCAATAT AGTCAAGTAG GCCAGCTGGC TCCTTCCTAC CCATTCCTGC 720 TGCGAGGCTC CTGCCCACGG ATGTGGAGTT TTGCTTCTGG CTTCCAGGAG CTTTTCTGGT 780 TTCTGTCTTG CTCTCTACAG GGGTCACTGG CCTGGGTCGG GAGGCTGCCC GCCATGTGGG 840 TGACCTTATG GAGCCAAAAG CCTTGAAGAT GCTACCGGGC CTGGGTTGGG GTCCTCAGGG 900 CTGAGCTAGA GGCCTGGCCA GTGGGAGGGG ATGGGTGCTC TTCCCAGTTC ACAGTGGGTC 960 AAAGGCAACA GCTCAGAACA GCTGCAGCTA AAGAGAGGAG AGGCAGGAGA GGAAGTGCAT 1020 TTCTTTGGCA AAGTATGTCT CCTGGGGCTG ACTCACACCC GTCTATGACC ACAGCCAGAA 1080 GCACATTCTG ACCAGCGTGT CCTGCAGAGT CCCCAGGCCT CGGTGAACAG GGCACCAAGG 1140 ACAGCTGCCT CAGCAGGGCC ACCCCACTCC GCTGGACATC CCCAGCTCCC CTCAAAGCCC 1200 CAGGCAGGCC CCTGTGCCCC TGGGTCCCTG TGGGTTTCTC CTCAGCAGCC TCAAATGAGG 1260 AAGTGAGGCT GAGGAGAGAA TGGGGGAACT TCTCTTCCCC CAATACATAT AGCAGCATAT 1320 AACATCAAAG ACACAGACAC ACAGACACAC ACACACACAC ACACACACAC ACACACACAC 1380 ACACACACCC CTTGCAGGTC AGAAGCAGAG TGGAGTTTGA TAGTAAGTGG 1430
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