Tag | Content |
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EnhancerAtlas ID | HS136-19754 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr8:142315680-142318690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr8:142317612-142317630 | GAAAGGAGGGGAAGAAGG | + | 6.19 | EWSR1-FLI1 | MA0149.1 | chr8:142317635-142317653 | GGAAGAAGGGGAAGAAGG | + | 6.2 | KLF16 | MA0741.1 | chr8:142318583-142318594 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr8:142318605-142318616 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr8:142318651-142318662 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr8:142318674-142318685 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr8:142318583-142318593 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr8:142318605-142318615 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr8:142318651-142318661 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr8:142318674-142318684 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr8:142318648-142318663 | ATGGCCCCGCCCCCA | + | 6.27 | SP1 | MA0079.4 | chr8:142318515-142318530 | GGGGGGCGGGGTCTG | - | 6.31 | SP4 | MA0685.1 | chr8:142318648-142318665 | ATGGCCCCGCCCCCAGC | + | 6.06 | ZNF263 | MA0528.1 | chr8:142317618-142317639 | AGGGGAAGAAGGGAAGGGGAA | + | 6.38 | ZNF263 | MA0528.1 | chr8:142317632-142317653 | AGGGGAAGAAGGGGAAGAAGG | + | 6.58 | ZNF263 | MA0528.1 | chr8:142317613-142317634 | AAAGGAGGGGAAGAAGGGAAG | + | 6.68 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_32282 | chr8:142315567-142316510 | Gastric | SE_32282 | chr8:142317257-142318560 | Gastric | SE_41505 | chr8:142317139-142318579 | Left_Ventricle | SE_42811 | chr8:142315290-142318545 | Lung | SE_47600 | chr8:142315618-142316088 | Pancreas | SE_47600 | chr8:142317351-142317717 | Pancreas | SE_47600 | chr8:142317922-142318500 | Pancreas | SE_65316 | chr8:142314855-142316840 | Pancreatic_islets | SE_65316 | chr8:142316933-142318155 | Pancreatic_islets |
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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: 3 | ID | Chromosome | Start | End |
GH08I141305 | chr8 | 142315662 | 142316644 | GH08I141308 | chr8 | 142317101 | 142317350 | GH08I141310 | chr8 | 142317381 | 142317530 |
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Enhancer Sequence | AGAAGGGCAC TGGCAATTTG GGGTTGTCTG CCACCTACAG TGCTTGTCAG TCACCCTCAC 60 TCGGTGCCAG GCCACAAGGC TGTTGGTCAC AAACCACCCC AGCCAGCCAC TGGGCGTCAG 120 GACCCTCGGG AAGAGCGGGA GAGGGCACTG GGATGCACCA CGGTCAGAAC GACAATCACA 180 GCCCGAACCC CTGCGCTGCA CTCCTCTGTC CTCCCCACCT CTCTCCTGAC AACACAGATA 240 CAATCCATTC ACCACCAAGC AACCTCAAGA TTGGCTGAAA TACCTTCCTC GGCTCCTTTC 300 CTCCATCGGG AAAGTGGGGA GCTGCCGCTG CCGCAGCCCT CTCCTTCCCT GCAGATCTGC 360 GGGGCGGGCT GGGGCGGGAT CTCAGAGCTC ACGGAAAGGA GGCAGAATCC GGTTTACAGG 420 CTTGCTCCGC CCCTCCCCCA CCCCCCTCCA ATAAGCAAAG TTAGAGGGTG TTACAAGCTG 480 CAAGACACAC ACCTTGGAGC TCACCCAGTC CAATCTCTGA TCTGCTTTCA CGATGCGACA 540 AGGGCCAAAG CTGCAGCACG CATCTCGGCA GGGCAGCAGG CCACTCCCCC CACGAGGCCC 600 GGGAGGTGGC CCTGGGCAGC CTCCCCACTC CCCGCCCTGT GAACACCTGG GCCAAAAAAA 660 CACACCTTTA AATACCCAGT GTGTATTTCA AACACATTTC AAACGATTTG CTTCTTTCCT 720 TTACAGCCAC TGCCACAAAA ACAATTAGCC TGAACGGGTG TGAAATCCTT GATGTGTAAG 780 ACGACCTAGT TCCCCAGCCT CTCTCTAGAA ACACATGAGT TCTTTACTGC GCCTGAGTCT 840 CCTCCACCCG GAACCTGCAG GGCTGCCTCT TCTCATCAAG TGGCTTCTGC AAAACCTCTC 900 CCAAGCATTT AAATAATCTC TGCTCGTTCT TTTAACAATA ATTCAAACCT AGCAGAAAAG 960 TGAGGACACT ATACATTTCT TTTAAGGACA GTGTGTGTTA CCTGCTCTGA TCCCCATGTG 1020 TTACACTCCC TAACCTGTAC ACCAATACTC CAGCTTTTTG TTTTCTTATT TTTTCCTAAA 1080 GCCAGCACAA AATAACAGAA GGATAAGATT CCTACCACAT TCTACCTGTC TGCCAATGAC 1140 ACAGGAAGGA TGAGACCGTC TGGGGAATGG AAGCGCAGGG CGCTCTCAGT AATGCTGGGC 1200 AGATGCAGTG GCTTTTCCCC AGCAGAAATG GGCTTCGATT CAGAATCTAC CAGCCCACAA 1260 GAATCATCTG ACCCCACAAC AATTAGTTCA ATCACTCATC TGGTAAACCC TCCTCGCTCC 1320 GGGTCATAGA CTGGAAAAGA CAGCCCCCAA AACAGTAATA AAAACGACAA GCCCTGTTTT 1380 GCTGGAGTCA GCTGAGGTAT CAGATGGGGG TCAGTGGCTA GGTCTGTGAA CCTGAAGCCA 1440 CACTCCATCA GTGACCCGCA CTGGAGAGAC ACAAACACCT CAGGCTCCTT AGGAGGTCAA 1500 GCGGCCCTTC CCAGCCCTCC CTAGCCCCCG CCTTCTAGAA TCATTCTGAA TAGCTAACCA 1560 GGAGGCTGGG CCCCGTGTGG ATCCGCCTCC GCTGGAAAAG CCGCTGCTGG AAGTGCTCCA 1620 ATCCAGAGCA GGATACCTGG GGGAGGAACG GGTTAAGCGC AAAGGGGAAA GGGGCAGCGG 1680 GTGCTGAGAC GCAGAAGGTG CGGGGACTTC TACAGAGCAG GGAATCTGGG CCCGGATGAA 1740 CTGATGCCCT GGCCTCTTTC CTCCAGGGAC AAGGTCGGTC TCAGGAAATC AAGGTATCTT 1800 CAAAGGGACA CAAGGGAGCG CAGTGCCGAT GAGACCGGGG CAGAGCCACA GTCTGGCGGT 1860 GCAGGCTGGG GGTCCGAGGC GGGGGACACT GGCTAGCAGT GCTGCCAGGG TCGTGTGTGC 1920 ACTGGGCAGA GGGAAAGGAG GGGAAGAAGG GAAGGGGAAG AAGGGGAAGA AGGGAGTGTG 1980 TTCGGTTGGG AGGACCGGTC CAGACAGAGG GGAGAGGGGG CCACTTCGCG AGTGGTGTAT 2040 CGCTGGTTGA ATTCTCATAA GTTAGAGATA GCAGGCAGGG GTTAGAAGGA CAAGACAGGG 2100 TCAGGACCAG GAGTTAGAGG CGCCAGGCTC CTCTCTGGGT AGAGAAACCG AGGAACTGGG 2160 GGCGGGGAGG ACTGATGGGT GCGAAAGCGG GCCGGGTCCA AATGAAGGCG CGCGCCCCGG 2220 GGTGGGGGCC GGGGTGGGGG GAATGAGGGA GGCTGCAGGG CTGGGGACCA GGGCAGGTGC 2280 AATCCGGAAA GAGGAGGCGG GAAGGAATTG GGGGGCCCTG AGGAGCCAGC GCAAGCCGGG 2340 TGGGGGCACG TCCCCTCCCC CGGAGAAGGT GCGGGGCTGG GGCTGCGGCG CGGACCCGAC 2400 CTGGAGGCCG AGGCTGTGCG GGAGGTGGGG GTGGGGAGGC TGCAGGTGCC CGGCGCCCAG 2460 GTGCGAGGTG CAGGGGGCGG CGGGGCAGGC GGCTGCGGGC GGCAGGCCAC TCACCTGTCT 2520 CCTCCGGCCG GGGCCGCGGG GGCGGCGGGG CGGCCGGGCC GGGCCGGGCA GGGGCTACGG 2580 GGGCGCGGAG CCCCGGGCGC ACCGGGGTCG GGAGGCGGCT GCGGGTCCGG GCGGGGGCTG 2640 CTCCCTCGGC CGGCCGGCCG GGCGGTCAGT CAGCGACGCG GGCGCGGAGA GAGCGCTGCG 2700 AGGCTGCGGC CGGCGCGCGG AGACAACGCC GCTTTATCGG GTCGGAAACA GCCGCTCCGC 2760 GCCGCTTCCG CTGACGCAGC GCCGGCCCCT GCGCCTCATG ACTATGCAGC ACCCGCCGCC 2820 GCGGGACGGG GATTCGGGGG GCGGGGTCTG CGCCGCGCGC GCTCATTGGC CTCCGCTGCC 2880 GCCCACCCCG CCCCCGAACG GCCGCCCCGC CCCCGCCGCG CCCCTGCCCC GCCCCCGCGC 2940 GCACCGTGGC TCCCGCCCCC GTCTCGCCAT GGCCCCGCCC CCAGCCATAA TCCAGCCCCG 3000 CCCCCGCCCT 3010
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