Tag | Content |
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EnhancerAtlas ID | HS184-06860 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:124924780-124925770 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr11:124924827-124924838 | ATTTTAATTAA | + | 6.62 | STAT1 | MA0137.3 | chr11:124924970-124924981 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr11:124924970-124924981 | TTTCCCAGAAA | - | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28104 | chr11:124924809-124925918 | Fetal_Intestine |
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| 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 |
GH11I125055 | chr11 | 124925019 | 124925710 |
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Enhancer Sequence | CCCTCCAGCC TAGGTGGCAG AGAAAGATCC TGTCTCTAAA ACAAATTATT TTAATTAAAA 60 AAAAGGAAAG AAAATAGAAA TTACTAAGGC ATGCTTTGGC ATACAGTGAA CATTTGGATG 120 TTAATTTTGA AGAAAGAAAC ATTTGGGCTT GAGAATGAGT TTCTAAGAAG GTAGAGTGGA 180 TCAGCACTCT TTTCCCAGAA ATTTCCATCT TGATCTTGAT TCCTGACTCT TGTAGCCTGT 240 TCTTCGTATA TTTTACAATA AGGAATGCCA ACAGTGTACT AGGAGCCAGG GCTCTCAGGC 300 TAGTGTTACA GAGTTGTAGG GAAATTCTAG GATGAAGTTT TTGCTGGGAC AAAGCAGATG 360 AAAGAGTTGA GTTTTTCCAG ATCTGGAGCT TACCTGTTGG GGATGCTGTA GACATCTAGA 420 GGCAGCAGGG ATATCTTCAG TCTTTATTGT GTAGTGCTGG TTTGTTTATT CAGACCTTCT 480 TTAATCTTAC TAATAAAACT CTTCACTTGA AGACCTTTCA GTCCTTGCCT GTGAAAGGCA 540 TGATTGTTCT TCTTGAAGTC ACATGCTTTT GATTTCTAAA CCCATTTCCA TTTTCATTTG 600 TTCAACCTGT TCTCCCTGTT TCATTCCTCT TGCTTCACGA TGTTACAATA AGAATGCATT 660 CCTAGTTGTA GACCTAAGGA GCAGTGTAAG GCAGGGAGGC ATTCCCACAA CTTCCTTGAG 720 CCTATCTTAG GCTTAATTAA GCCTATCATA GGCTTAATTG GTCACAGGGA CAGAGGTTAG 780 TCCCAAATGA TAAGAAGGAA TCTGTTTCTA CAAATGGAGT GGCCCTTGGG GAGAGCTTCT 840 GTCTCATCTT TCCACCAGCA TCACTGTGTG AACCAGGCAT GTCTGTTCTC TGCAAGTTAA 900 ATTTGTTTGT CTGAGTAGTA GGGAGGAGTA TTATCTCCTA GCCGTCTAGA GGTGCCGATG 960 AAGCTGTTCG ATAAAAGCAG AGTTACACGT 990
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