Tag | Content |
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EnhancerAtlas ID | HS024-16057 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr9:94908830-94911260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr9:94909571-94909589 | TCCTCCTTCCTTCTCTCC | - | 6.25 | EWSR1-FLI1 | MA0149.1 | chr9:94909559-94909577 | CCTGCCTTCCCTTCCTCC | - | 6.39 | EWSR1-FLI1 | MA0149.1 | chr9:94908971-94908989 | GGAAGGAGGGAAGGGGAG | + | 6.4 | EWSR1-FLI1 | MA0149.1 | chr9:94909563-94909581 | CCTTCCCTTCCTCCTTCC | - | 6.75 | EWSR1-FLI1 | MA0149.1 | chr9:94908967-94908985 | GAAGGGAAGGAGGGAAGG | + | 6.84 | EWSR1-FLI1 | MA0149.1 | chr9:94909575-94909593 | CCTTCCTTCTCTCCCTCC | - | 6.94 | MYCN | MA0104.4 | chr9:94910293-94910305 | GCCCACGTGGCC | + | 6.27 | MYCN | MA0104.4 | chr9:94910293-94910305 | GCCCACGTGGCC | - | 6.27 | Myod1 | MA0499.1 | chr9:94909799-94909812 | AGGGGCAGCTGCT | - | 6.18 | TP53 | MA0106.3 | chr9:94909728-94909746 | GACTTGCCTGGGCTTGTT | + | 6.65 | TP53 | MA0106.3 | chr9:94909728-94909746 | GACTTGCCTGGGCTTGTT | - | 7 | ZNF263 | MA0528.1 | chr9:94909630-94909651 | TCCTTCCCCCTTCCTTCCTTT | - | 6.02 | ZNF263 | MA0528.1 | chr9:94908963-94908984 | GAGGGAAGGGAAGGAGGGAAG | + | 6.18 | ZNF263 | MA0528.1 | chr9:94909556-94909577 | TCCCCTGCCTTCCCTTCCTCC | - | 6.56 | ZNF263 | MA0528.1 | chr9:94909571-94909592 | TCCTCCTTCCTTCTCTCCCTC | - | 6.58 | ZNF263 | MA0528.1 | chr9:94909534-94909555 | TCCCCCCCTCCTTCCTGCCCT | - | 6.59 | ZNF263 | MA0528.1 | chr9:94909563-94909584 | CCTTCCCTTCCTCCTTCCTTC | - | 6.86 | ZNF263 | MA0528.1 | chr9:94909575-94909596 | CCTTCCTTCTCTCCCTCCCTC | - | 7.94 | ZNF263 | MA0528.1 | chr9:94909579-94909600 | CCTTCTCTCCCTCCCTCCTTT | - | 7 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_02741 | chr9:94908477-94910639 | Astrocytes | SE_37838 | chr9:94907362-94917076 | HSMMtube | SE_39324 | chr9:94905779-94910548 | IMR90 | SE_46370 | chr9:94907846-94911556 | Osteoblasts | SE_56505 | chr9:94907669-94911466 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 94908932 | 94910146 | chr9 | 94910785 | 94910868 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I092145 | chr9 | 94907908 | 94911436 |
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Enhancer Sequence | AATGTCCAGA GAAGCCATGT TTTGGATGAA AAACTAGAAA GTGGGAGAGG CAGGGCGCAA 60 TCCTCTTTGA GTCTCCTGCT CCTGGTGTGG GACAGAGAAA GCTCCCAGGG AGAGCTGCTC 120 AGCTGCAGGC AGTGAGGGAA GGGAAGGAGG GAAGGGGAGG ACCCAGGCAG CATCCAGACC 180 AGGGTGGGGA AGAGAACTTA TTCTTAAGCA ACTTATTCTT AAGCAGCTTC CTGTTCTCTT 240 AGCCTTGAAC TTGAAGCCAG GAATAGGGAC AGGGATAGAA GAGCCAAGGC TTGGAGCCGC 300 TGGCCTATGC AGATGCACTT GCTTGTCCAG CAACAGTTGG ACAGGGCCTG GCCTGGGCAA 360 TGTGCTCCGG GGTGCATGGA AAATGTGGTC ATTCTTTGTC CGGGGGATTC TTCTTATTCC 420 CTCCCATTTC TCTTTACAGA GAATTTTACA CTTCCTTGCA GACACTGAAT TATTGTGTTA 480 AATTATTATA ACTTAATAGC TTGTGAAATA TACAAACAAC AAGATTATGC CGACATGGCT 540 GTTAGAAGAC AAGACAAATT AGCAGACTCA TGCTCATTTC TGTCATTGAA CAATTCGTCT 600 CATTCCTTCC TCAAGGCGCT GCCGTTTTCC TGCTCTCCGT CCGTGGGGGT GTTTGTTTAC 660 ACATCTCTCG CAAGAAAAGC GCTTCTCTCT GGCTTCCCTC TGCCTCCCCC CCTCCTTCCT 720 GCCCTCTCCC CTGCCTTCCC TTCCTCCTTC CTTCTCTCCC TCCCTCCTTT TCTCCCCGTT 780 CCTTTCTTCC CTTCTCTCTG TCCTTCCCCC TTCCTTCCTT TACTGATGTA ACAACCTTGG 840 TGTGCCGTGG CTAAGCCACA CTCCACCCCT GACCTGCGGG GGATGAGTCA AACGGTCAGA 900 CTTGCCTGGG CTTGTTCCAC GCTCCCCTGG CTAGACAGGC GTCTACACAT TCTCAGTTAG 960 GGGCTGGACA GGGGCAGCTG CTAGACAGGT CCTATTCTGG GCCTCTCTGA GAAAAAGTGT 1020 CCCTGAAAAG AAAGGGAGCT CCCACTTCCA TGGACCCTTA GCCATGCCAA GGGGCAGTAC 1080 CGGCTTTCTG CTGGTGCTGA TGAGCTGTGG TGTGAACTCA CGAAGGTCAG CTGATTCACG 1140 GGCCCTGGAT CTCTGCTCTC CTTCCGCTAA GTGGGACTCG GGCCAGCCTG CCATGAAGGA 1200 GGTAGCTGCT GCAGCTTTCA GGAAGGAACA CCAGGTGTCA ACCCCACCGG GTGGCCAACC 1260 CCACCTGGCT AGGACCCAGT CCCTGGTGGC TGCTCTCCCG AGAGGCGGGC AGGGCTGGGG 1320 CTAGGGGCTG TCCAGGAGTG TTCTGGACTG TCCCTTCGCC ACAATTCCCA CAGGCTGCTC 1380 AGGACCGAGG CTGAGACGGG CGACCAGGAC GGGATTGTAT GGCTGCAGGA GGCTACACAG 1440 TCCCAGGAGG CTGCTTCTAA GAGGCCCACG TGGCCTGCAT GGGGATGCGC CTGGCTGTCC 1500 AGCATGTGGT CATTTGAATT GTACATGTTT CACTGGGATG CCTACAGAAA AGTAGACAGA 1560 AGATGTGGAA AAAGTTTTTG AAATGTTGCA AACTTAGCTA CTTTTAAAAT AAAAAAAATA 1620 GCTTTATAAT TATAAAAGCA ATATGTAAAT CTTAAAATAA TTTGCTACAT TCTAGTAAGC 1680 ATCTTATGAT CTCTATGTGC CCTATAACAT TATGTTGTAT AGTTTAAATA TATACAATAA 1740 AATCTATTTT AAAAAATAGC AGGCAATTAA ATCTCATTTT AAAAAGAGTC AGTTTAACTC 1800 CCTTCTAATT TCTACCCCTC GTTTTCCCTC TGTGTGTGTG TATGTGTGTA TGTCATCTTC 1860 GTTAAATGGC TCAATGCATT CCGAATATTT TTTCCGTTGT CTTCATGATA TATTCATGGG 1920 AAGGGGAGTA TGTGGCTTAT TGCTGTTAGT TTATCAATAG AGAATGCTGG CCAAATGTCT 1980 TTAAGAGTAA TGACGATCTC AATAGCGGTA ATGACAGCTA CCACTTTCGG AGCTCCTCCT 2040 GCCTACCAGG CACCACTGGG GTCCCTCTCT GCAGCCCCTC ACGCCATCCT CCTAGTCACT 2100 TTCTGAGGTG TGTGTGGTCA TCCTCCCATT TGCAGGAGGG CTCTGAAGCA CAGGAAGGTT 2160 CGATACTTAC CCCATGGCCG GGATAAGATG GGCCAGGGCC AGGCTGTGAA CTAAGGCAGA 2220 GAAGGGGCTC TCCAGCACCT TTCCTGAGCC CTTGCCTCCT CTGCCTCTGC CCCATGGCCA 2280 TCTGGTGGGT GGACACAGCT AAGCCATGGC TAGAACCCAG CATTCTCATG ACTGCTTTAA 2340 CCATAGAAAA TCACAAGTTG CAAGCAACGG GACACACATT TACTTGTCTA CATTAGCACT 2400 TGTGATGAAG ATAATTCATG CTATTTTTTT 2430
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