Tag | Content |
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EnhancerAtlas ID | HS129-12538 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr14:104572020-104572980 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr14:104572709-104572720 | CTTCTGGGAAG | + | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_24938 | chr14:104569701-104575239 | Colon_Crypt_3 | SE_26694 | chr14:104570338-104576274 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I104103 | chr14 | 104569702 | 104576274 |
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Enhancer Sequence | GGCCTTCTGA CTGGCGGCGC TGCCTTAGTG CGGGGCTGCC TCGGGAGCTG CCTGTCCAGA 60 AGAAGGGCGG GTGAGTGGGG GCGGTGCTTG CTCTGGGCTC TCCCAGGCTC TGAGCACCAG 120 GGGTTCCAGG TGAGGAACCC GGAGGTGAGG GCCAGCCTTT GAGCACGTCC CCTGCACAAC 180 TGAGGTGCCC AGACCTAGGA AGGGGGGCTT TCGAGGCCTG GGGTCTGCAG GGGGATGGGG 240 CCTCCCTGGA CCCCGCAACA TGCCCCCTTG GCTGCTGGGC CAAACATCCA GGCCTGACAT 300 GGGGCCTGGC AGGCCAGACA GCCTTGCTCC CCACTGTGTG GGGTCCTGCC CCGGCCTCAG 360 TGCCTCGGTT TCCCCCTACA GGGATGGACC TGTCTTGTGA GCCATGTGCT GGAACTGCCA 420 CTTGCTGGGG CGGGTGATGG GCAGATGGAA AGGACTGGCG TGCATGGCCT GTTATTAGGG 480 TGGCTGCATA GGGCCTGAAT GCTGTAGGGA GGCAGGCCAG AGGCAGCAGC CTTGTCACCA 540 GGCCACGTTG TACCCGCTGG GTGTGGTGGC ACCTGTGGGG CCTCTGCCAG GACCGCTGGG 600 TGTGGTGGCC CCTGTGGGGC CTCTGCCAGG ACCGCGGCCT TTTGGCGTCT TGGGGAGCTC 660 CTGGTGCCCG GTGCTGGGGG CAGGTGGCTC TTCTGGGAAG GTGCAGCCGT GGGAACAGGG 720 CCTTCCTTCC AGGGGAGGGG TCTGGCTCTG CTTCCCACGC TCTCCTTATG TGGGTGACCA 780 TTCCGTCCCG ACGGCGGTGG GAGCAGACGG GGGAGTCTGG GAGGGTGGGT AGCAGGTACT 840 GGCCACACAC CCGTTGGGGA CAGGGCTGGA TGGTGGTCTC GTGGCCTGGC CTTAGCTCCA 900 GGGGAAGGGG TCCTAGGTGG GCCTGGATGG GGTGGGGTGG TGAGGCTCAA CCCCAGGCCT 960
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