Tag | Content |
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EnhancerAtlas ID | HS076-18746 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr14:103006350-103007350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Sox3 | MA0514.1 | chr14:103006999-103007009 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27866 | chr14:103005726-103007451 | Fetal_Intestine | SE_29137 | chr14:103005847-103007483 | Fetal_Intestine_Large | SE_68019 | chr14:102974923-103027639 | TC32 | SE_68438 | chr14:102968025-103022180 | TC71 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I102538 | chr14 | 103004742 | 103007648 |
|
Enhancer Sequence | GGCTGGGTGT GTGGAGGCCG CTCCTATGGC GGTGTGGGCG GTGCAGCTCA TTCCCCCGGG 60 GCTCCCAGCC TCCCACCCCC ATCCGGCCTC CTCCTCCAGA GCCTGGGGAC TGGTGGATGC 120 CTGCCAAGAA CGCCCACAGC CTGCCAGGAT GCGCAGGAAG CACACACACG CCTAATCCCA 180 CCCCCATTGT CATAGATCCC TCTTGATTCT GGGCCTGTCT TTCTGGGGGA AACTGAGGCC 240 CAGAGGGATT GAGGGCCCCC AAGGTCCCCG AGTCTCCAGG TGTACCTTGG AGGCTGTGCT 300 TTAGTGGGGC CTCCCCCGGC CTTCTTTGCA GTCCTGAGTG TGTGAAGGGG AGGAATCGGG 360 GGCTGCCAGG CCAGGAGCCA AGGCCGGGGG TGGGGAGCAG CTGGCAGGTG TCCCGGCAGG 420 AGGCCCGGCT AGGGGAGACC AGAACTCCTC TGCTCCTCCC TCCCAACGGC TTCCCACCCC 480 ACTCTACAGC AGGCCGCTGG CAGGCCCGGA AGGGCTTGGG AGCCGGAGGG TGCTTGCCGG 540 GGCTCCTGAA GGCCTGAGGA GCTCCTGAGG GACTGGAGGC TTCGGGCCTG GAAGGCTGGA 600 AGGCACTGGC CCTGCAGCTT GGTTCCCGGG GCTCCACGTG TCTGAATGCA AAACAAAGGC 660 GGCTCACAAT GAGAAGGCGG GTGCTGGGGA TCTGCCCCCG TCGTGCATGT GTCACCACAC 720 GGTGTCGAAG CGGACACCTG CCTCCGGGAT GAGCGCATTG GGCAACACTG CATGCTTTGC 780 ATTGGGAACA TGTTTGTGTG TGTGCGTTGG GGGTGTGTGT GCGGTGGGGG GCTATGGGCT 840 GGGATGTCCC TTGAGGTGAT CAGCTCTCTA CGTTCCGCAC ACACAAACAC ACAGTGTGAC 900 TGAGACACAC ATGTGAGTAT TGAGATCTCC AGGGCTGACT TCCTGCCGGA AGCATGCCCT 960 GGCCCCCGTC ACCTTGTGTG AAATTCCTCC ACCTGAGCAC 1000
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