Tag | Content |
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EnhancerAtlas ID | HS184-00145 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:10783800-10785980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr1:10784249-10784264 | TGAGAGCAAAGGCCA | + | 6.17 | HSF1 | MA0486.2 | chr1:10785937-10785950 | GAATGTTCTAGAA | - | 7.52 | MEF2A | MA0052.3 | chr1:10784279-10784291 | GCTATAAATAGC | + | 6.32 | MEF2B | MA0660.1 | chr1:10784279-10784291 | GCTATAAATAGC | + | 7.22 | MYCN | MA0104.4 | chr1:10784259-10784271 | GGCCACGTGGTC | + | 6.52 | MYCN | MA0104.4 | chr1:10784259-10784271 | GGCCACGTGGTC | - | 6.52 | NEUROD2 | MA0668.1 | chr1:10785441-10785451 | GCCATATGGT | + | 6.02 | ZNF263 | MA0528.1 | chr1:10784826-10784847 | GGAAGAGGAGGCAGAGGAAGG | + | 6.37 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_23090 | chr1:10783548-10785045 | Colon_Crypt_1 | SE_24724 | chr1:10782796-10784169 | Colon_Crypt_3 | SE_24724 | chr1:10784444-10785540 | Colon_Crypt_3 | SE_26723 | chr1:10782546-10784344 | Esophagus | SE_26723 | chr1:10784380-10784964 | Esophagus | SE_26723 | chr1:10784993-10785467 | Esophagus | SE_26723 | chr1:10785666-10786401 | Esophagus | SE_31374 | chr1:10781495-10788546 | Gastric | SE_40607 | chr1:10772324-10790002 | Left_Ventricle | SE_41555 | chr1:10781532-10785534 | LNCaP | SE_41555 | chr1:10785643-10788541 | LNCaP | SE_42099 | chr1:10779231-10788633 | Lung | SE_47486 | chr1:10783767-10784248 | Pancreas | SE_47486 | chr1:10784380-10785439 | Pancreas | SE_47486 | chr1:10785707-10786041 | Pancreas | SE_48119 | chr1:10782759-10788636 | Psoas_Muscle | SE_48591 | chr1:10773352-10788686 | Right_Atrium | SE_49447 | chr1:10781476-10784257 | Right_Ventricle | SE_49447 | chr1:10784422-10785425 | Right_Ventricle | SE_49447 | chr1:10785569-10788365 | Right_Ventricle | SE_54510 | chr1:10783384-10788141 | Stomach_Smooth_Muscle | SE_65281 | chr1:10783274-10785800 | 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: 1 | ID | Chromosome | Start | End |
GH01I010722 | chr1 | 10782912 | 10789847 |
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Enhancer Sequence | CCATGGCCTG GGTCCTTCAG GACTAGATGC CCAGGAAGCT CATCCAGCGG TCACATTTCC 60 CTCTAACTCC CCCTGCAACC TGGCTGCTCT CACGGTCAGC TTCAGTCCAC CCGTCTCAGG 120 TGGCCTCCCC AGTTCAGCAC TGCCTGGGTC ATGTGCCCCA GCCCCAGAGC CCACCTTCTC 180 CTCTTCTTTG GGGGTTCTTC CCGAGTCCAA ACCATGCCAG CAGGGGTTCA ACCCTAAACT 240 CACACCCAAC CGCTAGCACC TGCCCCAGCC TCCCATATCA CTTTGGATTC CTGGTGAGGA 300 CAAGTCCAGT TTTCCAAACC GACCTTGGAG CTCTTTGACC ACAGCACACT TTGGGAGAAG 360 GTGGAAGAGT CCTCCCCATC TTTGCCAAAA GAGGTGTCAG GCTAACGTTA CACCAGCTTT 420 AAAAATACCC CAGCACACGA TCCACAGGGT GAGAGCAAAG GCCACGTGGT CAGAGCCGGG 480 CTATAAATAG CCAGCAAATC ATTTCCCAGA GCCACGGCCC CCTCCCCAGC ACCAAGAACC 540 TTTCTGAGGA AATCAAAGTG AACGCAACTG TTACCAAGTC ACTACTAAAA TATTTACCAG 600 CCTGGCGAAG TGCCGAAGGT GCTTGGCACC GAGTGTTTGC TTATTTACAA GGCTGTTTTA 660 AAGGGTAGAA AGCAAAATAA GGTAACCTGA GCTATTAAAC CCGGGGGCCA GGTGGTACCT 720 ACCAGCTGTC AGCCACCCCA GGCATGTCGG GAGCTAGAAC AGTCCTGGTG GAGATTCCCT 780 TGAAATGGGT CAGGAAAGCA GAGAGAGGCT TTGGAGCCCA GGAATCACCT AGCCCTCAGG 840 GGTAGGGGCT CAGGGAGTGG GAGCAGAGAG TGTTAGAGGT TAGAGAAGCA CTTCTCCCCC 900 AGCCAAAGCA AGCAGGGCCT AGCACGAGCT CCAAGGTTGC CCCTGGTCTT CGCTCAGAGG 960 GGCACCCCAA GGGCACTGCC CAGCCAGAGG CAGGGGCAAG GGCCCTGGGA GGGAGAGGCA 1020 AGGCGGGGAA GAGGAGGCAG AGGAAGGCAG GTGGGGGGCT GGCTGGGAGC CTCGGAGGAT 1080 GACATAAGGG GGACACAGCC AACCTGGGGA AGAGAAGGTG CTCAACTTCT CTCTTTCTCC 1140 TCTTTCTCTG AAGTTTCCTT GTGGTTTGAA TTTAATTTTG ATTTTCTCAA CTTCAGCAGA 1200 TTGAAGTTGA AATAACCTAC AAATTACTTA ATGTGTTGTA AATCTGGGGG AATTCAGGAG 1260 TAATTGGGAC CACATGTTGG CCGGGAGGGA GCCCACAGAG GACGGAGGGA AGCAGCCCTC 1320 GCAGACGTGC AGGTGGCTGT TCTTCCCTGG AGGGAGGGGG CTTGGGCTCC CCTCGGTGGG 1380 GGTAGGATTC CCTAGTTGGC CAGGGAGCCC TGGATGGATA CGGCGAGAAC GTGTTAAGAC 1440 CAAGGAGTGA CCATGTCACT GCCCAGGGCA GCCCGGTGAC CGTGGACACA GGGCGGCCAA 1500 GTAGGCTGGG TGCCAGGCGT CTGCCAGGCC CCTCCACCGT GCCAATGCCA ACACCGTGGC 1560 CGCCTCCCGC TGCATGCGTG TGGCTGTCAG CTGAGCTCCC CTCCCGCCCT CCCTCTCCGG 1620 CAGGCTCCTC TCAAGTACTG AGCCATATGG TTCCAGTTAA GCTCCATATT TTTCCTTGTC 1680 GATTGAAGAG ACACACTTTC CTCTTTGCCA GACAGTTTGC AGATTGCTCT GTTGGCTCAA 1740 TTTCTTATTG GATTTCTCAA AAAACCTGAC ATTTTAAATT AATTTACAGC CACAACAAAA 1800 AGAGTTCAGA ATTTTAATGG TGTTGTAAGT AATTTTTAGG TAATCCACTC CAGATTTTGA 1860 TATTAACCTT TGAAACTGGA GTTCATTCAG CTACCATGTT ACAATCCAGT CACACTCCAG 1920 GCCTGGGGGA GGCCAGGCTT GGGGAGGAGG TGGAAGCCAG GTTCTGGAAA GCCCTTTTTT 1980 TTTTTTTACT AGGAGACCCC AGAGAGGATG ATCCTGGGGA ACCCTGGACA GGTGAGTGAC 2040 AAGACAGCGG CAGTGGGGTG GGGAGGGAAT GGCAAGGGGG GCCTGAAGAC AGCAGGGCAG 2100 GTGTAAGAGA GTCATTGAGG GGGCCAGAGG GCCTGCCGAA TGTTCTAGAA GGATGGGCCG 2160 GACTTAGGAG GGGGCAGCAT 2180
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