| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05869 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:68898560-68899890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr11:68899711-68899721 | GGGGCGGGGC | - | 6.02 | | SP1 | MA0079.4 | chr11:68899709-68899724 | TAGGGGCGGGGCTTA | - | 6.38 | | SP2 | MA0516.2 | chr11:68899708-68899725 | GTAGGGGCGGGGCTTAC | - | 6.61 | | SP4 | MA0685.1 | chr11:68899707-68899724 | GGTAGGGGCGGGGCTTA | - | 6.54 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32040 | chr11:68898474-68900187 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I069130 | chr11 | 68898426 | 68899882 |
|
Enhancer Sequence | GCCTGTTGGC TTGTGGTCCC TGCCGGCTCT TGTCCTGGAG GTCCTCTTAG CATCGTGCTG 60
GTCCTAAACA GAGGCTCAGA AGGCTGTCCC CAACCTCTGC TGTCCCGGAG CCCCTTCCCT 120
CTGGGTGTCT GTGCATCTAG GCCAGGCCTT GCTCGAGGAG GGTGCAGGCA GCCTGGCAGG 180
GGAGCCTCTA GGCATGAGCT GGCCAAGGTC CCTGGCACTG TCCGAGCTGC CCAGGGGTGG 240
CCCGGAAAGG TTCCCAGACT GCGATATCTC GATGGGCCAC CGTGTCTTAG CATGGGCCGC 300
CTGGTTTTCC ACAGAAGATG TCTGGCCAAT CCTAGAGCCA CCAAATTTCC AGGCAGTGGG 360
CTGTCCCATG TTCCCAAGAA CAACCCTGGG CTGGCTGCCA CACGGCTACT AGCTGTGTGT 420
CAGGCCTACG TAGATGTACT TTGCATACAC TATCTCCATT AGAGACTGGG GTGTAGATAG 480
GATTGCAATC CACAATTCCC AGATGAGGAA ACTGAGGCAC AGAGAAGCTG GTAGGTGGCC 540
CAGCCATGAT GGGAAGCTAG GGTGGGAAGC GCTGAGGGAG CAGCTCTCCT CCTCAGGTAT 600
TCAGACCTGC CTAATGGTGC AAATGCCTCA GCCACATTCC TGCCTCTAGG TGGGGCATCT 660
TGCACGTGTG TTCCCGAGGG CTTTGCCTGC TGGCTGGGAA TTCCTGGGCT AAAGAGCTGA 720
GCACTTGCAT TTTCTGACTC CCATAACTGT TGGTCAGAAC CGAGGTGGGG TGTAGAGGTC 780
CTGAAGCCAG CCCAGAAAGG TCTGGTTTCT GACCCACCCA CCAGCTGTTG CCTTTCCCTG 840
CAGACCGGGA AACGCGGTGT GGACTCTCAC TGCTTCTCCG GCTTGGAAAC GGCGTTCCTG 900
TCTTTGCCTT CTCCCTGGGG CTGGAATCCC TCCTGGACAG GCCTAAGGCA TGTCATGGGT 960
CCCCCTCCCT CCCTGCTGTA ACCCCAGAGC CCCCATGGGG AACCCGCAGC TTCCATCATC 1020
CTCAGGGGCC CAGTGTCCCA GGAGGGGACT GTGGAGAGGT GTTTGTACTC CTGGGTGTGT 1080
CTGGGCTGCC ACTTGCCCAG GGTCTGGGAG GTGACCTTGT GCCAGATGGG GCTGGAAGCT 1140
CCCTGAGGGT AGGGGCGGGG CTTACCCTGG TGCACCTGTG TTGCACGTGG CCTCGGATCT 1200
CGTTCCTGTC ATGTCTTGGG GTCTTTTCTA TTCCCAAGGT TGTCGTAGGA AGGCGTTTGC 1260
TGACAAATGA GACCTGGCTC CCTCCAGATT CTGATTCTGT CCCTCTCTTC GTGAGCCTGG 1320
ATGGGTCGGG 1330
|
