Tag | Content |
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EnhancerAtlas ID | HS184-04963 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:2223270-2224500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr11:2223672-2223693 | TTCCCTCCTCGCCCCTCCCCC | - | 6.32 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_56724 | chr11:2222752-2227371 | VACO_400 | SE_57716 | chr11:2222825-2224599 | VACO_503 | SE_65606 | chr11:2222980-2227005 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 2223839 | 2223970 | chr11 | 2224165 | 2224215 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I002201 | chr11 | 2223156 | 2226663 |
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Enhancer Sequence | CCCAGGTGTC TGCCAGGCCC TGCCCAAAAA TGCAATGTCT GGGCAGCAAG GAGGCTGAGG 60 CCAGACCCCA CCCTCATCCA TGCCTGGAAC CTGCATCCAC GTGGCAACCC CTCCCTCCAA 120 ACCCAGCTCA TGCCAGGGCT CAGAGCATGG TGGAGAGGGT AGCCCTGGGC ACCTGGGGCA 180 TGGCAGGACT GCCCTGCCTG CCCCGCCTGC CCCGCCCTGG CCCGTGCCTG CAAGAGCCAC 240 CTAGGGAAGG CTCCTTCACC TGGCCCTGGG CCTACACTCC ACCCAGGAAT GTCCTGCACC 300 CCTGGAGTGT GGAGATGAAG GTTACGGGGT CCAGCCTCTG GGCACCGGGA CATCTGGGGT 360 AGGGGCTGAA GGCCATTCAA AGCCCCTGCC CCGAAGTCTA CCTTCCCTCC TCGCCCCTCC 420 CCCACCCACC CTGGGGGAGG TTTGTAATCT TCAGTGTCAT AACCTGTCAG GCCTGTTTGG 480 AAGGGAAGGG CCGCCAGCTT CCTACCAGGG AGCAGGGAGC TCAGGCGTTG GTTAGAGAAG 540 AGGTGAAGCG TGCACAGGAA GCGTGCGGGG CCCCCCTGGG CATGGGGGAG GGGCGCCGGC 600 CGACGGGAGC TTGGGCACGT GCTCACACAC GGGACTGGAC CGTGTGTCAC AGCAAGCCTG 660 GGTAGGTGCA GACAGGTCCG CGCGTGTCAC CTGCGCAGTG CACAGGGGCC TCTGCTGCGG 720 ACGCAGGGCC TGCCGGAGTG ACTGCCTGGC TGCCCAAGAT TCCAGGGGTT CCACTCCATC 780 CGGTGCTGAG TGGTGCCCCC CACCCCAGAG ACCTGGGACA GCCGAGAAAT GGAGGAGAGG 840 AACCCACCCA CCCAGCCCTG TGGCCTCCAG GCTTGACTTG GGTGCAGCTG GCAGAGGCCC 900 TGCCCCTCTG GCTGTCTCCC TCCTAGAGGG GTCTAGGAGT TTCAGGAACT GGGGACCGAG 960 GGAGGTCTTC TGCAGAGACA AGAGGGCGCA GGGCGCAGGC CAGGAAACCC CTTCACCTGC 1020 AGAGCCATCG GTGTGGGGAG GTCAGCCACG GGGTGTCTTG GTGTCTCAAG GGGGCCTTAG 1080 GTAGAGCTGT TCACTCCCTC CTTGTGGCCC CCCGAGGCCC AGGAGGGACC TGGAGCCCAT 1140 GTCCCAGGAG TGCCCTTGGG AAGGTCAACT CCAGGAACCC TTGCAGCCCG AGGCTAGGGC 1200 TCTGAAGCTG GGATGGGCAG CGGGGGCCCT 1230
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