Tag | Content |
---|
EnhancerAtlas ID | HS026-34809 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr9:136756990-136759220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr9:136758430-136758448 | GAAAGGGAGGGAGGAAAG | + | 6.45 | EWSR1-FLI1 | MA0149.1 | chr9:136758434-136758452 | GGGAGGGAGGAAAGAAGG | + | 6.84 | EWSR1-FLI1 | MA0149.1 | chr9:136758442-136758460 | GGAAAGAAGGAAGGAGGC | + | 7.41 | EWSR1-FLI1 | MA0149.1 | chr9:136758438-136758456 | GGGAGGAAAGAAGGAAGG | + | 7.87 | ZNF263 | MA0528.1 | chr9:136757113-136757134 | AGAGGAAAAGGGGATGGAGGA | + | 6.05 | ZNF263 | MA0528.1 | chr9:136758409-136758430 | TGAAGAGGAAGGGAAGAAGGA | + | 6.11 | ZNF263 | MA0528.1 | chr9:136757106-136757127 | GAGGGAGAGAGGAAAAGGGGA | + | 6.12 | ZNF263 | MA0528.1 | chr9:136758427-136758448 | GGAGAAAGGGAGGGAGGAAAG | + | 6.22 | ZNF263 | MA0528.1 | chr9:136757096-136757117 | GGTGGAGAGAGAGGGAGAGAG | + | 6.32 | ZNF263 | MA0528.1 | chr9:136758432-136758453 | AAGGGAGGGAGGAAAGAAGGA | + | 6.34 | ZNF263 | MA0528.1 | chr9:136757093-136757114 | AGAGGTGGAGAGAGAGGGAGA | + | 6.37 | ZNF263 | MA0528.1 | chr9:136758421-136758442 | GAAGAAGGAGAAAGGGAGGGA | + | 6.3 | ZNF263 | MA0528.1 | chr9:136758436-136758457 | GAGGGAGGAAAGAAGGAAGGA | + | 6.49 | ZNF263 | MA0528.1 | chr9:136757206-136757227 | GGGGAAGGAGAGGGATGGGGG | + | 6.4 | ZNF263 | MA0528.1 | chr9:136758412-136758433 | AGAGGAAGGGAAGAAGGAGAA | + | 6.64 | ZNF263 | MA0528.1 | chr9:136757196-136757217 | TGGGGAGGAGGGGGAAGGAGA | + | 7.49 | ZNF263 | MA0528.1 | chr9:136758424-136758445 | GAAGGAGAAAGGGAGGGAGGA | + | 7.93 | ZNF263 | MA0528.1 | chr9:136757199-136757220 | GGAGGAGGGGGAAGGAGAGGG | + | 9.15 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_42028 | chr9:136756943-136759071 | LNCaP | SE_65284 | chr9:136756799-136758993 | Pancreatic_islets | SE_68854 | chr9:136757213-136759168 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 136757600 | 136758000 | chr9 | 136757373 | 136757600 |
|
| Number: 2 | ID | Chromosome | Start | End |
GH09I133893 | chr9 | 136759068 | 136759862 | GH09I133891 | chr9 | 136756928 | 136758994 |
|
Enhancer Sequence | GAGGCATGGG GATGGAGTTG GGAGAGGTGG GGATAGAGGG CGTGGAGTGA GAATGGAGGA 60 GAGGGGTAAA AGTAGTGGAT GAGTGGACCA AGGCATTCGG GGGAGAGGTG GAGAGAGAGG 120 GAGAGAGGAA AAGGGGATGG AGGAGAGGGA CAAAGGACGG GGTGCCAGGG GTGTGGGGAG 180 ACGAAAGGGA TGAAAGAGGT GGGGTGTGGG GAGGAGGGGG AAGGAGAGGG ATGGGGGCAT 240 TGGGTACGGG GTGGAAGGGA CCCAAGGGCG GGGTGGGGGA TGATGGAACA GAGGCCAGTG 300 GTGCAGGGGA GGGGTAGAGG GGGATAAAGG GGAGATGAGG GGAGGGGTGG GGATCAGCAA 360 GGGGCCTGCT CAGGTGCCAG TGGGAACAGG TGTCCCGGGT TGGCTGCATG GGGCTGTGCT 420 GCTAGGAAGT GAGGCCTCCT GGTGCTTCCG CAGGGCTGCA GGGCTTTGTG AGCCAGGAGT 480 GTCCTTTGAA CACAAACAAG CCTCTGTTTA TTTTGGAAAT GTGGGGGCTG AGGAGGTGGG 540 GAGTGAAAGC TGACACTCAT TAGAGCACCC TTACCAGTGC ACACACCTCT GTCTATAAGC 600 ACACTGGGGA GGAGACAGAA TTAAGTCACT TGGCCAAGAT CATCCCAGGG GTCAGCAAAA 660 ATCAATCTGC ATCAATCCCT GGGCCCCATG CAGGGCTCGG CCAAAGGGCA GCCGAGCACC 720 TAACCCGCCT GGCCGTCCCT CCTGGGTCTC CGTGCCTGAA TCGGGCGTCA GAGTCCAGCA 780 GAGACAACTG TCCTTCGGCT CCAACAGGGA CACAGGGGCA CAAGGAGCTC AGGAGGGCAG 840 GGCAGGCTGA GCTGCAGGGC TAGAGGGAGG AGAGGACTCA CAGGCCAGAG ATGCAAGAGG 900 AGGGGCGAAT CCGGGCCAGG CTTCAGCTCA GAGGCCATTG CAGACGAGAA AAGCGGACCT 960 GGCCCAGCCT TGGCAATAAA AAGCATTCCA GGTTCTTGTA AGGGGGAAAG AAAGAGCCAA 1020 GCGGTCTCCA TCCACGGGGA ACTTGCCCGA GCCCACCCCC AGAATTATCA TCAGGATGAT 1080 GTCTCACAAA AAGACTTCAA AGTGAGACCA GGAACACCAT CTTCCTGGTC GTGAGGAGCA 1140 GGTTTTGCTG GGCGGTGAGG GGCCCTGGCC CTTAGACACG CAGTAAGGCG GACTCAGCTG 1200 CCCTTTCTCT CAGAGGACAG CACGGTCCAA GATCTATGGC TCTGAGTCCG ATCTGGGCAC 1260 TTACCAGACA GCCTGAGTCC CACCTCCCGC GAAGACTCCT CTTGCCACCC TCCCAAATCC 1320 ACAGGCCTCT AAAGGTGGGA GTCTGACAGC CAGGTGCCTT CAGGCTGTGG AGGGGTCACA 1380 CAAAGGCCCC ACAGCTGCAG GGTGGAGGGT GGAGAGGGCT GAAGAGGAAG GGAAGAAGGA 1440 GAAAGGGAGG GAGGAAAGAA GGAAGGAGGC TCGGGTGGCG AAGGCGGCGG CAACAGCAGC 1500 TGGGCCTCAG CTGGTCCTCG GTCCCACAGT CGGGCAGCGC CACGGTGGGG CAGCGTGGAG 1560 GAGGAGGCCC TAGCGACAAC TCTGGGGTCC TCAGGTGGCA AGGGACCTGC CCCGCACGGC 1620 CGCCTACCAG GGGCGAGCCC TCCCTCCCCG GCCTTCATAA AAGCAAAATC TAGACAAAGG 1680 AGCCAAGATG GCCGACACCC ACTCCGGCCA GCTCCAAAGG TCACCTTCAA GAAACGGAGT 1740 TTGCAGGAAG TCAACGGTGC CTGCAGAACA GGGGCGAGCA CCCAGCCCAG CCAAGGCCAG 1800 GAGGAGCCCA AGCCTTCCTC CGTCGCCACA CGGCAGCTTT CATTGCCTGA ACCTCGGAGG 1860 GTGGCGGGAC GGTGATTCCA CCCACAGCCG CGATGACCGA GGCCCAGCAT CGCAGCAAGT 1920 GGCAGAGAAG CCAGAGTCCA ACTACCGCCC CTGAAACCCA CCGCACCTGA CCCACACAGC 1980 AGCGGCGAGA GTCGGGCGCC CACGTGTACC ACACACACAG TTGAATGCTT TACTGGACCT 2040 CACGGATCCT CACAGACCTC TGGAAAGTTC TGTCGTAATC TCCACCTTAC ATCTGCAGAA 2100 ACTGAGGCTC GGGGAGAAGG AAGACAGTAA CGGGCCCAAG GCCACCCCGC CAAGCAGCAT 2160 GACATCCACC CCACAGCCCA TGGCTGAGAA TCCATCCCCC ACTCCCCGCC TCCACTGCCC 2220 GTCAGAATTC 2230
|