Tag | Content |
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EnhancerAtlas ID | HS184-02404 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:209978510-209979290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:209978709-209978729 | CCCCAGAGCAACCACACCCC | + | 6.16 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27309 | chr1:209977673-209980487 | Esophagus | SE_27823 | chr1:209977468-209983975 | Fetal_Intestine | SE_35823 | chr1:209974126-209984775 | HMEC | SE_64223 | chr1:209974556-209984573 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 209978699 | 209978810 | chr1 | 209979142 | 209979287 |
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Enhancer Sequence | CTCTCTCTAT CCATCTCTTT TCCCTGACTT CCACTCTTGA CATCCACCAA GAGAACAGGT 60 TGGAACAGGA TGACCCCTTT ACCACAAAGC AGGCTCCCTG TAAAGAGTGA CACCTCAGGC 120 CTCCTTTCCA AGTCAGGCCT GGGAGACTTT CCCCATTCTC CACACCACCC TCCAGCCCCT 180 TCGGGCAAAG AGGGCCCACC CCCAGAGCAA CCACACCCCA GCGCCACCCT CCCCAGCACC 240 TAGCTCCGCT CCTTGGAAAT CCAAGGTTGT CTCCCAGGCC CAGGGCGAAG GGCCTAACTG 300 TGCCAAACAG ACTCAGGGAG GGAAGACAAA CCGCCAATGC TCCAAAGCTC CTGGCCACCC 360 TCACTCCAGT TTCCCAAAAC GCCCACTAGG ATCAAGGACC TGCGGACCTG GGAAGTCCCC 420 TCTCTGGGAC ACAGGGGCCA GCCGCAAGTT GGTAAGACTG AAGGGGGCGC GGTGCTTTAG 480 CTCTACCGGA TAGTGGGGTT GTTGACGGCC GAGAGCAGTG CCCTCCGCTT CGGCGGTGGG 540 GGTAGGGAGA GTAGACACAA GTGTAGATTC GAGAGGGGCC TAGCGCTACA GAACTGAGGC 600 CGCCCCAAAG CTATCTGGAA AAGGGCGACA GGCACCCAGC CCCAGTGGGT ACCCACCCCA 660 AACACACAGA TGCCCCCAAG CAAGTTCTCT CACCCCCTAC AAACTCCGGG GATGGGTCCT 720 ACCCCACCCA CGGGGGAGCC TCTCCTCCCT CAAGCTGGTC CCCAGAAGTT GGCGTACCCA 780
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