Tag | Content |
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EnhancerAtlas ID | HS012-01119 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr1:230887260-230890140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F1 | MA0024.3 | chr1:230888924-230888936 | AATGGCGCCAAA | + | 6.11 | E2F4 | MA0470.2 | chr1:230888923-230888937 | AAATGGCGCCAAAG | - | 6.57 | EWSR1-FLI1 | MA0149.1 | chr1:230889589-230889607 | CCCTCCCTCCCTCCCTCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr1:230889593-230889611 | CCCTCCCTCCCTCCCTCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr1:230889582-230889600 | GCTTCCTCCCTCCCTCCC | - | 6.36 | FOXP1 | MA0481.2 | chr1:230887511-230887523 | AGGTAAACAGAA | + | 6.14 | IRF1 | MA0050.2 | chr1:230887263-230887284 | GGAGAGAAAGAGAAAGAAAGA | - | 6.48 | IRF1 | MA0050.2 | chr1:230887345-230887366 | AGAAAGAAAGAGAAAGAAAGA | - | 6.76 | KLF5 | MA0599.1 | chr1:230889862-230889872 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr1:230889885-230889895 | GGGGCGGGGC | - | 6.02 | Myod1 | MA0499.1 | chr1:230888862-230888875 | AGCAGCTGCCCCC | + | 6.03 | SP1 | MA0079.4 | chr1:230889883-230889898 | AAGGGGCGGGGCTTC | - | 6.3 | SP2 | MA0516.2 | chr1:230889882-230889899 | GAAGGGGCGGGGCTTCC | - | 6.26 | SP4 | MA0685.1 | chr1:230889881-230889898 | GGAAGGGGCGGGGCTTC | - | 6.66 | ZNF263 | MA0528.1 | chr1:230888329-230888350 | GAAGGCTGGGGGAGGGGAGGG | + | 6.08 | ZNF263 | MA0528.1 | chr1:230888780-230888801 | GGTGGAGGAGGAAGAAGAGCA | + | 6.74 | ZNF263 | MA0528.1 | chr1:230887295-230887316 | AAAGGAAGAAGAGAAAGAAAG | + | 6 | ZNF263 | MA0528.1 | chr1:230889593-230889614 | CCCTCCCTCCCTCCCTCCCTT | - | 7.05 | ZNF263 | MA0528.1 | chr1:230887602-230887623 | GGGGGAGGGGAGGGGGAGGGG | + | 7.49 | ZNF263 | MA0528.1 | chr1:230889589-230889610 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 | ZNF263 | MA0528.1 | chr1:230889585-230889606 | TCCTCCCTCCCTCCCTCCCTC | - | 8.08 | ZNF263 | MA0528.1 | chr1:230887607-230887628 | AGGGGAGGGGGAGGGGGAGGG | + | 8.24 | Zfx | MA0146.2 | chr1:230888313-230888327 | CGGGGCCAGGCCTG | + | 6.24 | Zfx | MA0146.2 | chr1:230889485-230889499 | CAGGCCCCGGCCCA | - | 6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_32194 | chr1:230887396-230890088 | Gastric | SE_33557 | chr1:230879014-230891230 | H2171 |
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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 |
GH01I230750 | chr1 | 230885992 | 230891172 |
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Enhancer Sequence | GAAGGAGAGA AAGAGAAAGA AAGATAGAAA AAAAGAAAGG AAGAAGAGAA AGAAAGAAAG 60 AAGAAAGAAA CAAAGAAAGA AAGAAAGAAA GAAAGAGAAA GAAAGAAAGA AAGAAAGAAA 120 GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA AGGGTGGCTT 180 TTCCCTTTGT GAATTATTCA CTGTGCTTAG TAGAGGAAAG TGTGTCTTCG GCTGAGCCCC 240 GATGATGTAC AAGGTAAACA GAACAGTCCC TGAAAGCAAA CATTCCAGGG TGCTTGGCCC 300 TTAGTGCTCC AGGAAAACCA CCTGGTGGTA GGGCTGTGGG GTGGGGGAGG GGAGGGGGAG 360 GGGGAGGGGT CTGCGTGCCT CCCTCGGGGC TTCAGGCAGC AGTCTAGGTT CACTTCAGGT 420 TTGTCAAGAC CCCTGCAATT GAGACACCTC TGATCGTCCT ATCACAGGAC TGTAGCTTCA 480 GGTAACCCCT TCCTCATGGC CTCCCAAGCA ACATTTCACA GGAACAAATG TACATCCAGG 540 ATCGACACGC ACATGCAGGA CACTCACACG TAGACAATGC TCCCAAGTGC ACATGCAACC 600 AGCATACATG TGGAGCATGC ACAAGCACAC ACGTGTACCA CACCTGGGCA CACACAACAA 660 GGCAAGTCAC AGGCACCTTG CACATGTGGG CATGTGGGCC GTCAGCATAC ACACCACTCC 720 CAGGCATCTA ACCCAGGCCC ACCGCCTAGC TGCCCCTTCC ACACATGCGT CCGCAGAACC 780 CCCTGTGACT GGCACGTGTG CACACCAATT CCCAGAAACA CTGACCCACA GAGGAGTCGG 840 TCACACATCC AGACACCTCC CCAATTTATA CCCGATGGCT AATTTGTGTT TACTTGGAGA 900 GTTTCTGAGT TTTTTCCTTT TGTATTTTTC TCCTCATTGG GTGCGATCTG GTTTAAAACA 960 AAAACAAAAA CAGACCTCTC CTGAACAAAA CAACCAATTG CAAGATAGGA GCTGGGAGGC 1020 GGTGGCAGCT GCAGGCACAG TTGGTACGGT TGGCGGGGCC AGGCCTGCAG AAGGCTGGGG 1080 GAGGGGAGGG GCAGGGAGGA TGGGAAGGAG GCGGGCATCC GGGAACAGCC CTGCCCCAGG 1140 AGCTAGCACA GCCTGCTGGG CAGGGATCTG TGGCTTTTGG AGTACATTTT ATGTCCACTT 1200 GAGGAGTGAG TAGCATTGGC AGTGGGGGCA TTGCTTGCCA GGGCTATCCC CTGGCAGGGG 1260 CTGGGCAATC AAGACAGGGA GGGCTTGGGG GACTCCTGGG TTTCCCTTCG GGCAGGCACA 1320 TTCTGCAGCA AGCCCAGAAT GTCTAAGCTG GTGACAGATG AGGATGCAGC CGTGAGAAGT 1380 TAAATGGCCC ACCCTGAACC CTACTGCTGA GCGGGGCAGG CTATTCCTGG GACTCTATTG 1440 AGGCCCACTG ACATGGTCCT GGTTTGCATT GTCCTTCTGG GCTCAGCTCA GAGCCACCTG 1500 CAAACTCCTG CGCTAGCCAA GGTGGAGGAG GAAGAAGAGC AGTGTGCTTC CTACAGATGA 1560 GAGGGGTCCG CACAGGCAAG CCAAGCCAGG ACCCCAGAAC TGAGCAGCTG CCCCCCACCT 1620 TCACTCCCTT TCCAGCCACC ACGGAGATCA GAGTCATTTA ATGAAATGGC GCCAAAGCTA 1680 CCTGGAGCTG GGGGTGGGAA TGCAAAGACG TGTGAGACCT GGCAGAGGAC AGGCCAGCAT 1740 TTGGGAGGTC CTTACTTCTG CCGGGCCTGG GGTTTTGGCG CATCTAAAAA CACCCCGTGT 1800 TCTTCAGAAA TTCTCCTGGC CAAGCTTTCT TGAGTATTTT AGACACTAAT GCCACACATA 1860 GCTCTCCCTG GGCAGGCGCC CCTGGTGTCT GTCACTCCTC CAGGTTGTCA CATCCTGGGG 1920 AATGCAGAGA GAGCACCAGC ATTTGAAGCT TCTGCTCTTG GTCCTGATAA TCCCCTTGAC 1980 TTCAAAGAAA TCTCTGTCCT GCCTTTGATT CTTTGGGACA CAAGATGAGA GGAGAAGCAG 2040 GGTGCTGAGA AGCCTGAGGA AGACAATTCA AAGCAGAGGT CTCTCGGGGA AGGCGGCGCA 2100 GCTTGAGCTC CCCACGTGGC GTCCGCCCAG ACACTGCTGG AACCTTCCAC CTCCAGCCCA 2160 GGCCCCTCCT CAGTCCTGGT GCCTGGAAAA GTGGGAAGAG GTGGGAAAAA TCCTTCACTC 2220 CTCTGCAGGC CCCGGCCCAG TTAACTCACC ACCCCTGCAG GGTGAGCCAG AACGGGCCTC 2280 GCTGCCACAG GATTGGCTGT TACCTCTCCC GAGACCGGCC CGGCTTCCTC CCTCCCTCCC 2340 TCCCTCCCTC CCTTTGTTTA GGTCTGTGCT CCTCTGCTTC CCCCAGAGAC GCCTCCCCTG 2400 CTGACTGCTG TAGCTAGCCT TGCCCCATCC CACCCCTTCC CTCTCCATCC TCGCTCTTTT 2460 CTCTCCTGGT TTATGGTTTG TCTCTTCCTC AAATGCAATT TGCAAAACTC TCCTGAACGA 2520 AACAACAGCT TCTGGGAGGT GGTGGCAGCT GCAGGCACAG TGGGCGCCGT GGGTGAGGCC 2580 AGGGCTGAGG CAGGCTGGGG GAGGGGCGGG GCAGGAGGCT GGGAAGGGGC GGGGCTTCCG 2640 AGAGCACCGC CCTCCGCGTC CAGGGCAGCT CCACCAGGGC AGGGGCTTTC CCTCTCTCTT 2700 TGTTGTCGTC CAATGTCAGG AATGGAGCCC AGCAACTCAA AGAGTGGAAG AATATATGCA 2760 TATCATAAGA TTGCTTTCTA CACTTTTTTG TTCATGTTTT ATAAATACCC CTCCATATTG 2820 TATATGTATA TATTAATATG TATTAATGAT TACATTAATA CACATAGTGT ATGTGCTTAT 2880
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