Tag | Content |
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EnhancerAtlas ID | HS183-14036 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr9:133374950-133376360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr9:133376167-133376180 | GATAAATTAATTA | - | 6.11 | SOX10 | MA0442.2 | chr9:133376336-133376347 | TTCTTTGTTTT | - | 6.62 | Sox3 | MA0514.1 | chr9:133375311-133375321 | CCTTTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr9:133375992-133376013 | CCCTCCGTCACCTCCACCTCC | - | 6.18 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33497 | chr9:133371778-133378014 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I130497 | chr9 | 133372415 | 133377081 |
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Enhancer Sequence | CCCTCAGGTG AGAAGCTCAG GGCCCTGACG GGCCTTCAGA GCCTCCAGGT GTAAAGGGTA 60 GGCTTTGAGA GCCCCCAGGT GTAAAGGGTA GGCTTTGATG CGACCTTGAC TGCTGCCCTG 120 CCCTGCCCTG CCCTGCCCTA GACAAACCCC ACTTTCCTGT CCATCTGCCC ATAGCATCCT 180 CAGAAGCATG CTTTGATAGC CGACAGTAAC AGAGGGTCCT AGGCATTGGG GTCCTAGGTT 240 CCTGTGTCCC ACCGGGTGCC TCTGATACTT GCCCTCCCCT CCCGCTAAGC CACAGGGACT 300 CCACTATGAG CTCCTTTGCA GGGCAGGTTA AACAAGGAAA TAGCATAGAG GTGGAGAGAA 360 GCCTTTGTTT TCTGTCACCA TACCTGAGCT GTAGGTCTAG CTGGAAGCCA TCCTAGCCAC 420 GTGGATCTCC ATGGCCCAGG AGGGTGGTGC ACGTCATCTG AAGTCACTCA GACCTTTGAT 480 CCTCTGTGAG TCACCAGTAA GAGTGTCAGC TGTACCTGCC TCACAGATGC AGTGAAGGTT 540 CAATATGAGC CTGTGGAAAT CAAGCATGCG GCTCAGGCTT AGACCCTGGC ATGCAGGAAG 600 AGCCAGGGGC AGTGCCAGCA GCAAGCACAC TCAGCCCAGG GCCGGTGTGC TCAAGGGCAA 660 ACAGGGTCGT TTGTCACCAG CAGCTAACAT AGACTAAGCT GCTCTGGGAC ACTCTCCTAG 720 GATGTCTCAT TTAATTCTTA CACAAAATTT GCAACTCCCC GGGAACAGGC TGAGTGGTTA 780 AGTAACTTTC CAAGGGTCAC ACAGCTAGGA GGTGGTGGAG CTGAGTCCGG AGGGCCTGTC 840 CTGCTGTGGG TTCTCCATCA CCAGCTCCCT TCTCATGGGG ATTGGAGTCT AGAAGAAGAT 900 GCAAGTCAGT CTCCTCTTGC TAACAACATG CCCTGGGCAC AGAGCCATCA TTTTCTCCCA 960 GAGCCAGTCT CTTGTCCCTG GAGGCACCTC ATGCCCCGAG AGATGTTGAA GCCCGCCCAT 1020 CTGCCCAGGG TCCTCTCCCT TCCCCTCCGT CACCTCCACC TCCCCTGCCT CCTGCGCCCT 1080 CTGTTTGTAT TTTATGACTC TATAAACCCT TTTAAATGGC CCAGAACAAA CAGGGCTTAC 1140 ATAGTGGCCT CTTCATTTCT CCTATTGCCA GTTAAACGCT TTGTCTTCAA CAATGACAAA 1200 CAATGTTTTC CCCCTAAGAT AAATTAATTA CATTATCCTG ATTGGAGGGC AGGAGGGGCC 1260 AGGGCGGGAG AGGGAATAGA AAAAAAGGCA ACTTCACACA CATCTTAACA AACAGCTGCC 1320 CCAGCCACCC CAGCTCTGCC TGAATTAATT GAACCCAGTG TGTGTTGTTA TTGTTAATTT 1380 ACATTTTTCT TTGTTTTGAA TCTGGTTTAC 1410
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