Tag | Content |
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EnhancerAtlas ID | HS129-24674 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr3:10968310-10969990 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr3:10968759-10968769 | ACTTGGCACC | - | 6.02 | STAT3 | MA0144.2 | chr3:10968834-10968845 | TTTCCCAGAAG | - | 6.62 | Stat4 | MA0518.1 | chr3:10968831-10968845 | CGGTTTCCCAGAAG | - | 6.13 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27487 | chr3:10966886-10970885 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I010925 | chr3 | 10966887 | 10970885 |
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Enhancer Sequence | TCTGTGCTCG GCCCTCCCTA GAGGCCCCTT GCCAACCTCC CCCTGCTTGG CAGCCTCCTT 60 CCCTGGCGAA GGGGGTAGAC CTGGAGCTAG TAACTCACCC ATGCACTCGG TTTCCCTTTG 120 TTGCCACACA GCACGCAGGC GCTCGCTTCC CGCACTGAGC ACACTCCAGA CTCCCATCCC 180 AGGTCCCCGG CCTCTTTCCC AGACCATTCC CCCAACAGTC CCTGAAACCC ACCCTTTGCC 240 TGCTGGTCCT CACAGCTGTT TTCCCTAGGA GCCCTGGAGA ACTTCCCCCA GCCACAGCCT 300 CCCCGCCTCG GAGACTGGGG TCTCTTGGCC AACCAGTGCT GTGCTGTGCA GGGGCCTCTG 360 CAGGCAAAGC AGTCAGACCC CCAGGGAGAC ACACCCAGCC CAGCCTGTGG GAGTGCCGCC 420 CTCACCCATG ACCTTCTGCC AGTTGAGTCA CTTGGCACCC AAGCCCCACA GCCAGTATAT 480 CTGTCAAGCC AGCCAAGTCC AATTCAATTT CTTCCTCTGA TCGGTTTCCC AGAAGCTGCT 540 AAGCCAAATC ACCGGGTGTT TCTGCTGATA ATCTTCCCTT ATTGTTGCTG TTGCGGGCAG 600 AGGTCTCGGA GGGATTGGCA GCTTATGCGT GACAGGCCAG GCCTGCCTGG CAGAGGGAGG 660 CAGGGGCTGG GGCCCCGGCT CGGCGAGTCC CTGGGCTGAG CTAAACCAGC AGTTGGGCCT 720 GGGGGCCCGA GGTCTGGCAC AAAAAGTGGC GGCCACTCTG CCTATCCCCA TGCGTGCTGC 780 CCTTGCTGTG TGCCTTGGAT ATATTCTCAG TTCATTGTCA CAATAACCAC ACGGGCTGGG 840 GGCTCCTTTC ATTGTCTGCA TTTTATAGAA GAAGAAACTG AGGTTCAGAG ATACTGAGTG 900 ACTTGCTCGG TCGTGTACCC GGGCCCGTCT GCCTCTTGGC CTACACACTG CAGTGTCTCA 960 TCAGTTTCAA TCCTGGATAA ACAACCTCCT TTGCATCCCA TCCTCTTCCC TAGGACCTGG 1020 AGAAAGGATA GACAGAGCCA GCCCTTGCTG CTGAGGCGGA GCAGCTGCGA GGCCATAGCC 1080 TGGGCTTGAG TCCCAGCCCC ATGACTTGCC AGCTGTGTGC CTTGGGCTAG TCACCTCGCC 1140 TCTCTGTGCC TCATTCCCTT TGTCTGCACA AGGAGTATTG AAACACCTTT TCTGGGGAGG 1200 CAGAGGTGAA TCAGAAAGGA TTTGGAGCCG ACAAATAGCT CCAGGGAAGG GGTGCTTCCC 1260 AAAAAGGTGG CTGGCAAAAT AACCCTTAAC TCCTCCTCCC TCCCTCAAGG CAGGGCAGTG 1320 GGGTGGGTAA AGCCCAGCTC TGGAGCAAGA TCACCTCGTT CAAATCCAGG CTTTGCCACT 1380 TATCGCCTGG GTGACCTTGG GTAAATTGCT TACTCCCTCC TCTGTGCTTC TGTGTCTTCA 1440 TTTACAAAAT GGGAATAATA ATAGTACAGA CCATGTAGAG ACTACATAAG TTAATGTATG 1500 CCAACTGCCT AAAACAGCCT GGCACATCGC AGGTATGATA TGTTTGCTAT TATTCGTGTT 1560 ATTATTATTA ATTTAGCAAA CATTTCCTGA GCCTCTCCCT CCTCTGTGCC AGGGGCCCTG 1620 AGCTAGACAC AGGAAATAGA CAGATGACAA TGATGTGGCC CCTTCCCTCC AGGATCCCAC 1680
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