Tag | Content |
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EnhancerAtlas ID | HS183-00496 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr1:230887570-230890040 |
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 | 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 | chr1:230889593-230889614 | 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 | AGGAAAACCA CCTGGTGGTA GGGCTGTGGG GTGGGGGAGG GGAGGGGGAG GGGGAGGGGT 60 CTGCGTGCCT CCCTCGGGGC TTCAGGCAGC AGTCTAGGTT CACTTCAGGT TTGTCAAGAC 120 CCCTGCAATT GAGACACCTC TGATCGTCCT ATCACAGGAC TGTAGCTTCA GGTAACCCCT 180 TCCTCATGGC CTCCCAAGCA ACATTTCACA GGAACAAATG TACATCCAGG ATCGACACGC 240 ACATGCAGGA CACTCACACG TAGACAATGC TCCCAAGTGC ACATGCAACC AGCATACATG 300 TGGAGCATGC ACAAGCACAC ACGTGTACCA CACCTGGGCA CACACAACAA GGCAAGTCAC 360 AGGCACCTTG CACATGTGGG CATGTGGGCC GTCAGCATAC ACACCACTCC CAGGCATCTA 420 ACCCAGGCCC ACCGCCTAGC TGCCCCTTCC ACACATGCGT CCGCAGAACC CCCTGTGACT 480 GGCACGTGTG CACACCAATT CCCAGAAACA CTGACCCACA GAGGAGTCGG TCACACATCC 540 AGACACCTCC CCAATTTATA CCCGATGGCT AATTTGTGTT TACTTGGAGA GTTTCTGAGT 600 TTTTTCCTTT TGTATTTTTC TCCTCATTGG GTGCGATCTG GTTTAAAACA AAAACAAAAA 660 CAGACCTCTC CTGAACAAAA CAACCAATTG CAAGATAGGA GCTGGGAGGC GGTGGCAGCT 720 GCAGGCACAG TTGGTACGGT TGGCGGGGCC AGGCCTGCAG AAGGCTGGGG GAGGGGAGGG 780 GCAGGGAGGA TGGGAAGGAG GCGGGCATCC GGGAACAGCC CTGCCCCAGG AGCTAGCACA 840 GCCTGCTGGG CAGGGATCTG TGGCTTTTGG AGTACATTTT ATGTCCACTT GAGGAGTGAG 900 TAGCATTGGC AGTGGGGGCA TTGCTTGCCA GGGCTATCCC CTGGCAGGGG CTGGGCAATC 960 AAGACAGGGA GGGCTTGGGG GACTCCTGGG TTTCCCTTCG GGCAGGCACA TTCTGCAGCA 1020 AGCCCAGAAT GTCTAAGCTG GTGACAGATG AGGATGCAGC CGTGAGAAGT TAAATGGCCC 1080 ACCCTGAACC CTACTGCTGA GCGGGGCAGG CTATTCCTGG GACTCTATTG AGGCCCACTG 1140 ACATGGTCCT GGTTTGCATT GTCCTTCTGG GCTCAGCTCA GAGCCACCTG CAAACTCCTG 1200 CGCTAGCCAA GGTGGAGGAG GAAGAAGAGC AGTGTGCTTC CTACAGATGA GAGGGGTCCG 1260 CACAGGCAAG CCAAGCCAGG ACCCCAGAAC TGAGCAGCTG CCCCCCACCT TCACTCCCTT 1320 TCCAGCCACC ACGGAGATCA GAGTCATTTA ATGAAATGGC GCCAAAGCTA CCTGGAGCTG 1380 GGGGTGGGAA TGCAAAGACG TGTGAGACCT GGCAGAGGAC AGGCCAGCAT TTGGGAGGTC 1440 CTTACTTCTG CCGGGCCTGG GGTTTTGGCG CATCTAAAAA CACCCCGTGT TCTTCAGAAA 1500 TTCTCCTGGC CAAGCTTTCT TGAGTATTTT AGACACTAAT GCCACACATA GCTCTCCCTG 1560 GGCAGGCGCC CCTGGTGTCT GTCACTCCTC CAGGTTGTCA CATCCTGGGG AATGCAGAGA 1620 GAGCACCAGC ATTTGAAGCT TCTGCTCTTG GTCCTGATAA TCCCCTTGAC TTCAAAGAAA 1680 TCTCTGTCCT GCCTTTGATT CTTTGGGACA CAAGATGAGA GGAGAAGCAG GGTGCTGAGA 1740 AGCCTGAGGA AGACAATTCA AAGCAGAGGT CTCTCGGGGA AGGCGGCGCA GCTTGAGCTC 1800 CCCACGTGGC GTCCGCCCAG ACACTGCTGG AACCTTCCAC CTCCAGCCCA GGCCCCTCCT 1860 CAGTCCTGGT GCCTGGAAAA GTGGGAAGAG GTGGGAAAAA TCCTTCACTC CTCTGCAGGC 1920 CCCGGCCCAG TTAACTCACC ACCCCTGCAG GGTGAGCCAG AACGGGCCTC GCTGCCACAG 1980 GATTGGCTGT TACCTCTCCC GAGACCGGCC CGGCTTCCTC CCTCCCTCCC TCCCTCCCTC 2040 CCTTTGTTTA GGTCTGTGCT CCTCTGCTTC CCCCAGAGAC GCCTCCCCTG CTGACTGCTG 2100 TAGCTAGCCT TGCCCCATCC CACCCCTTCC CTCTCCATCC TCGCTCTTTT CTCTCCTGGT 2160 TTATGGTTTG TCTCTTCCTC AAATGCAATT TGCAAAACTC TCCTGAACGA AACAACAGCT 2220 TCTGGGAGGT GGTGGCAGCT GCAGGCACAG TGGGCGCCGT GGGTGAGGCC AGGGCTGAGG 2280 CAGGCTGGGG GAGGGGCGGG GCAGGAGGCT GGGAAGGGGC GGGGCTTCCG AGAGCACCGC 2340 CCTCCGCGTC CAGGGCAGCT CCACCAGGGC AGGGGCTTTC CCTCTCTCTT TGTTGTCGTC 2400 CAATGTCAGG AATGGAGCCC AGCAACTCAA AGAGTGGAAG AATATATGCA TATCATAAGA 2460 TTGCTTTCTA 2470
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