Tag | Content |
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EnhancerAtlas ID | HS040-22891 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr20:60802820-60804180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr20:60803019-60803037 | GGGAGGAAGCAAGGATGG | + | 7.09 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41928 | chr20:60802424-60804553 | LNCaP |
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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 |
GH20I062227 | chr20 | 60802813 | 60803731 |
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Enhancer Sequence | CACACACAGG CCGTTGGGGC CCTCCCCTCC AGCAGCTGAG GTCAGCATAG GCAGGGGCCT 60 GGTGGATCTA GTGGAGGGCG ACAGACAAGA ACGTGGGACA TGTGGCCAGC ACACCTGTGC 120 TCACCGCCCA GGGCTGCTGG AGGGCTAGCC CCGTCTCTGT CCACCCCCTG CCTCCCGCCT 180 GGGTGGGGTA GTCTGTTTGG GGAGGAAGCA AGGATGGCCA CGGCGGGGGC ACACTGGAGG 240 CCCGTTGTGA GTACTGTGCA GGCCGGTCTC CATCTGGCTG CCGCCTGGAT CCGTTCTCAG 300 GGTAAGGCTG AGAGGCCAGC CTTACCCTGG AACCTGAAGC CTGGTGAGGA GGTGGCCCCT 360 CCTCCTCCCT CTGTCCCCAC CTCCTGCACC TCCATGCCCC TCCCCAGACA CACGCCCCTC 420 ACGCTCTGCC CCACCCGGCA CCTTCCCCTA TGGGTGCCTC CTCCCAGAAG CCTTCAGGGT 480 TATTCCAGGT CTTCCCATTG CCTGTGCTGT TCCCAGAGCT GCTGGCCGTG GTCCCAGGTA 540 GTGTATGCCC TCACCCCTAG GGCAAACGCA GCGCCCTGAC CCCTCCTGGA GCCTTGGGTC 600 CTCTTCCCCT GCAGAAGGTC GGGAAGAGGC GCCACGTGGA GGAGCTGAGC AGTGCAGGTG 660 GGCTCAGGGA GCCTCGTCCT GGAGGGGGAG TCTGGGCCCT ACGAGGACGA GGACAGAGAT 720 GGGGACAGGG ACGGGGACGA CCCTCTCTGT TGACTCCCTG GAGTCCCGCA GATCCAGGGC 780 AGCTCCTGGG GACCTGGTGC CTGCTGGAAA AACTAACCCA GCTTTGATCA GTGCTGGGGC 840 CGGGACCCAG TGAATGTGGC CGCCCCCGTG TGCTGGGGGA GGAAGGATGG GGGCTCCCAA 900 GCAGCAGGCA AAGAATGCAT GCGTGTGCGT GCGTGTGTCT ATGTCTGCGT CTGTCAGTGT 960 ACACGTCTCT GTGCATCCGG GTATGTCTGT GCGTGTCTCT CTGGGCTATG TGTGTGTGCA 1020 CGTGCGTCTG TGGGTCTGCG GGTGTGTCTG AGGGTGTTTG GTGCGAGCTG TGACAGAGGT 1080 GTCGGGAGGA AACTGACACT GTCCCCTTCT GCCCTGCAAG GGACAGGTCA GGGTGGGAGA 1140 AACAGTTCCT CCCTCCACAA GGCCCTGAGC CAGGGCAGGG GGCGACAATT GCTCTAGAGG 1200 CAGACTCCCC TCCCCTGGGT CTGGGCACGA ATCACTGTCA CTTGCTGCCC ACACGCCTTT 1260 CCATACACAC ACACACTCAA CACTCATCCC ACACACACTC GCACACGCAA CACTCACACA 1320 CTCAACACTC TCACACTCAC CCCACACACA CTCACACACT 1360
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