Tag | Content |
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EnhancerAtlas ID | HS183-02474 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr17:73980520-73981910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:73981823-73981838 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6(var.2) | MA0728.1 | chr17:73981108-73981123 | GAGGTCAAGAGTTCG | + | 6.24 | SOX10 | MA0442.2 | chr17:73981609-73981620 | TGCTTTGTTTT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27115 | chr17:73978558-73981720 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 73980617 | 73981099 | chr17 | 73980717 | 73981041 |
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Enhancer Sequence | CCAGGCTGGA GTGCAATGGT GCAATCATAG CTCACTGCAG CCTCGACCTC GCAGACTCAA 60 GCGATCCTCC CATCTCATCC TCCCAAGTAG CTGGGATTAC AGGCATGCAC GACCACACCC 120 GGATAATTTT TATATTTTTA GTAGAGACGA GGTTGCCCTC AAACTCCTGA GCTCAAGTGA 180 TCTGCCCGCC TCAGCCTCCT CAAGTGCTGG GATTATAGGC ATGAGCCACT GCACCCAACC 240 TTGTTCTGAT TGTTTTGAAG CATTTGTAGC TTCTAGCAGG TAAGCAAAGC CCAGTCCAGA 300 GTCACAGTCT GTTCCTGTCA AGGAACAGAG TTCAGTGGTA CTGCCCCAGA GCTACCAGCA 360 TGAGTCTCAC TTGCCAGCTA TGATCAGGAC CTTCCACCAC GTTATCTGCA CCATAGCCAC 420 AGGCAGTCTC TGTCTCTTTT GCTGACAAAC AGAACAGTTC TTCCTGGCAC TATGTGCCTG 480 AGAGGGTGCA AGAGGAACGT GTTGATGAAG AGAGTCAAAT TGGGCAAGGC GCGGTGGCTC 540 ATGCCTGTAA TCCCAGCACT TTGGGAGGCC AAGGTGGGTA GATCATCTGA GGTCAAGAGT 600 TCGAGACCAG GCTGACAAAC ATGGTGAAAC CCCATCTCTA CTAAAAAGCA CTGGGATTAC 660 AGGTGTGAGC CACCATTCTG GGCCACACAT AGCTTTTTAA ATATTGTTTT GGTTTATTAT 720 TATTTTGAGA CAGGGTCTTA CTCTATTGCC GAGGCTACAG TATAGTGGTG TGATCATAGC 780 TCACTGCAGC TTCAACCTCC TGTGGTGGTG ATCCTCCTGC CTCAGCCTCC TAAGTTGCTG 840 GGACTACAGG TGAGAGACAC CACACCTGGC CCATTTTTGT ATTTTTTTTG TGGAGATGGG 900 CTGTTGCCAT GTTGCCCAGA CTGGTCCCGA ATTCCTAGTC TCAAGGGATC CACCTGGCTT 960 GGCCTCCGAA AGAGCTGGGA TTACAGGCAT GAGCCACTGT GCCTGGCCTA ATGTTTTAAT 1020 TTTTTCATAG AGATGAAGTC TCACTATGTT GTCAAGGCTG GTCTGTGTTT GTTTTTTGTT 1080 TGTTTGTCTT GCTTTGTTTT TTGAGACGGA GTCTCGCTCT TATTGCCCTG GCTGGAGTGC 1140 AATGGCACGA TCTTGGCTCA CTGAAACTTC CACCTCCTGG GTTCAAGCTA TTCTCCTGCC 1200 TCAGCCTCCC AAGTAGCTGG GATTACAGGC ATGCGCCACC ATGCCCGGCT AATTTTGTAT 1260 TTTTAGTAGA GACAGCGTTT CTCCATGTTG GTCAGGCTGG TCTTGAACTC CTGACCTCAG 1320 GTGATCCGCC CGCCTCAGCC TCCCAAAGTG CTGGGATTAT AGGCATGAGC CACTGCACCC 1380 GGCCATGTTT 1390
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