Tag | Content |
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EnhancerAtlas ID | HS182-21679 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:94908540-94910400 |
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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I092145 | chr9 | 94907908 | 94911436 |
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Enhancer Sequence | CGGGCCCCTG CAGGGGCTAC AGATGAGGAG GCAGAGAAAC AGGCGGCCTT AACAGGGGAG 60 AGCCAGCCTT GGAGAGGATG TATTGTGAAT TGGGGGTGGG GGTGCCAACG TGCCAGGTCT 120 CATTTCTCAC TTCCAAGGCC ACCCTTCCCT GGCCCAGTCT TAGTCGCCCT TTCTAATAGA 180 TTCTAAGAGT TTGACTCCTC CTTCCGGAAA CTTGGGGTTT GTGAGTTCTA ATCTTCAGTC 240 TCTCAGTTGC TATGAGACCC TGTGCAAGTC CCAAAACTTC CCTGGACCTC AATGTCCAGA 300 GAAGCCATGT TTTGGATGAA AAACTAGAAA GTGGGAGAGG CAGGGCGCAA TCCTCTTTGA 360 GTCTCCTGCT CCTGGTGTGG GACAGAGAAA GCTCCCAGGG AGAGCTGCTC AGCTGCAGGC 420 AGTGAGGGAA GGGAAGGAGG GAAGGGGAGG ACCCAGGCAG CATCCAGACC AGGGTGGGGA 480 AGAGAACTTA TTCTTAAGCA ACTTATTCTT AAGCAGCTTC CTGTTCTCTT AGCCTTGAAC 540 TTGAAGCCAG GAATAGGGAC AGGGATAGAA GAGCCAAGGC TTGGAGCCGC TGGCCTATGC 600 AGATGCACTT GCTTGTCCAG CAACAGTTGG ACAGGGCCTG GCCTGGGCAA TGTGCTCCGG 660 GGTGCATGGA AAATGTGGTC ATTCTTTGTC CGGGGGATTC TTCTTATTCC CTCCCATTTC 720 TCTTTACAGA GAATTTTACA CTTCCTTGCA GACACTGAAT TATTGTGTTA AATTATTATA 780 ACTTAATAGC TTGTGAAATA TACAAACAAC AAGATTATGC CGACATGGCT GTTAGAAGAC 840 AAGACAAATT AGCAGACTCA TGCTCATTTC TGTCATTGAA CAATTCGTCT CATTCCTTCC 900 TCAAGGCGCT GCCGTTTTCC TGCTCTCCGT CCGTGGGGGT GTTTGTTTAC ACATCTCTCG 960 CAAGAAAAGC GCTTCTCTCT GGCTTCCCTC TGCCTCCCCC CCTCCTTCCT GCCCTCTCCC 1020 CTGCCTTCCC TTCCTCCTTC CTTCTCTCCC TCCCTCCTTT TCTCCCCGTT CCTTTCTTCC 1080 CTTCTCTCTG TCCTTCCCCC TTCCTTCCTT TACTGATGTA ACAACCTTGG TGTGCCGTGG 1140 CTAAGCCACA CTCCACCCCT GACCTGCGGG GGATGAGTCA AACGGTCAGA CTTGCCTGGG 1200 CTTGTTCCAC GCTCCCCTGG CTAGACAGGC GTCTACACAT TCTCAGTTAG GGGCTGGACA 1260 GGGGCAGCTG CTAGACAGGT CCTATTCTGG GCCTCTCTGA GAAAAAGTGT CCCTGAAAAG 1320 AAAGGGAGCT CCCACTTCCA TGGACCCTTA GCCATGCCAA GGGGCAGTAC CGGCTTTCTG 1380 CTGGTGCTGA TGAGCTGTGG TGTGAACTCA CGAAGGTCAG CTGATTCACG GGCCCTGGAT 1440 CTCTGCTCTC CTTCCGCTAA GTGGGACTCG GGCCAGCCTG CCATGAAGGA GGTAGCTGCT 1500 GCAGCTTTCA GGAAGGAACA CCAGGTGTCA ACCCCACCGG GTGGCCAACC CCACCTGGCT 1560 AGGACCCAGT CCCTGGTGGC TGCTCTCCCG AGAGGCGGGC AGGGCTGGGG CTAGGGGCTG 1620 TCCAGGAGTG TTCTGGACTG TCCCTTCGCC ACAATTCCCA CAGGCTGCTC AGGACCGAGG 1680 CTGAGACGGG CGACCAGGAC GGGATTGTAT GGCTGCAGGA GGCTACACAG TCCCAGGAGG 1740 CTGCTTCTAA GAGGCCCACG TGGCCTGCAT GGGGATGCGC CTGGCTGTCC AGCATGTGGT 1800 CATTTGAATT GTACATGTTT CACTGGGATG CCTACAGAAA AGTAGACAGA AGATGTGGAA 1860
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