Tag | Content |
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EnhancerAtlas ID | HS007-17702 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr9:133375110-133376360 |
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 | CCATCTGCCC ATAGCATCCT CAGAAGCATG CTTTGATAGC CGACAGTAAC AGAGGGTCCT 60 AGGCATTGGG GTCCTAGGTT CCTGTGTCCC ACCGGGTGCC TCTGATACTT GCCCTCCCCT 120 CCCGCTAAGC CACAGGGACT CCACTATGAG CTCCTTTGCA GGGCAGGTTA AACAAGGAAA 180 TAGCATAGAG GTGGAGAGAA GCCTTTGTTT TCTGTCACCA TACCTGAGCT GTAGGTCTAG 240 CTGGAAGCCA TCCTAGCCAC GTGGATCTCC ATGGCCCAGG AGGGTGGTGC ACGTCATCTG 300 AAGTCACTCA GACCTTTGAT CCTCTGTGAG TCACCAGTAA GAGTGTCAGC TGTACCTGCC 360 TCACAGATGC AGTGAAGGTT CAATATGAGC CTGTGGAAAT CAAGCATGCG GCTCAGGCTT 420 AGACCCTGGC ATGCAGGAAG AGCCAGGGGC AGTGCCAGCA GCAAGCACAC TCAGCCCAGG 480 GCCGGTGTGC TCAAGGGCAA ACAGGGTCGT TTGTCACCAG CAGCTAACAT AGACTAAGCT 540 GCTCTGGGAC ACTCTCCTAG GATGTCTCAT TTAATTCTTA CACAAAATTT GCAACTCCCC 600 GGGAACAGGC TGAGTGGTTA AGTAACTTTC CAAGGGTCAC ACAGCTAGGA GGTGGTGGAG 660 CTGAGTCCGG AGGGCCTGTC CTGCTGTGGG TTCTCCATCA CCAGCTCCCT TCTCATGGGG 720 ATTGGAGTCT AGAAGAAGAT GCAAGTCAGT CTCCTCTTGC TAACAACATG CCCTGGGCAC 780 AGAGCCATCA TTTTCTCCCA GAGCCAGTCT CTTGTCCCTG GAGGCACCTC ATGCCCCGAG 840 AGATGTTGAA GCCCGCCCAT CTGCCCAGGG TCCTCTCCCT TCCCCTCCGT CACCTCCACC 900 TCCCCTGCCT CCTGCGCCCT CTGTTTGTAT TTTATGACTC TATAAACCCT TTTAAATGGC 960 CCAGAACAAA CAGGGCTTAC ATAGTGGCCT CTTCATTTCT CCTATTGCCA GTTAAACGCT 1020 TTGTCTTCAA CAATGACAAA CAATGTTTTC CCCCTAAGAT AAATTAATTA CATTATCCTG 1080 ATTGGAGGGC AGGAGGGGCC AGGGCGGGAG AGGGAATAGA AAAAAAGGCA ACTTCACACA 1140 CATCTTAACA AACAGCTGCC CCAGCCACCC CAGCTCTGCC TGAATTAATT GAACCCAGTG 1200 TGTGTTGTTA TTGTTAATTT ACATTTTTCT TTGTTTTGAA TCTGGTTTAC 1250
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