Tag | Content |
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EnhancerAtlas ID | HS105-06873 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:212655690-212657080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr1:212657046-212657056 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:212657046-212657056 | GGCACGTGCC | - | 6.02 | MEF2C | MA0497.1 | chr1:212656484-212656499 | GAGCTAGAAATAGAA | + | 6.18 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35302 | chr1:212655268-212663203 | HeLa |
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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 |
GH01I212481 | chr1 | 212655167 | 212663350 |
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Enhancer Sequence | GTTTGGTTGA CTTCAAATAT GTGGCATGGG TGAGCCATTT CCTCAGGGCA TCTTCAGGAT 60 CTGACTGAAG GATCCAGCCC AAGGCCCTGT GGGTTTGAGG GGAGGAGAGG ACACAGTCCA 120 GGAGCCACCT TTACCTGTGG ACTTGAGGCT CCTTCCAGCC CTGACCAATG ACAGGAGCAT 180 GGCAGAGGGA AACCAAGAGA TTCTGAAGGA GGAGGAATGT TCAAAGGGCA AAAAGCTCTC 240 AATTTTATTA ACTCTTGAAT AAACAACTCG TCCTTAGGGA CAGATGAGTA ACCCAGGAGG 300 AACCCAACTC TATGAAGGGC AGAGTTGCAT TCTATTGCCC TAGGAAACAA CAAGGGAAAA 360 TGAGATTCCT CTGTTATCCT GAACATGGAT TATTCTTGTC CCCCCTCCCT TTTTTTAAAT 420 CATTAGAGGG ATTTATTTCC TTTCCGGAAG AGTCACTCTT CTGCGGTCCT TCCACACCCA 480 GCTTTGGACT GGGCCACCTG GCAAGGGTGT GAAGTGGACT TGTGGTTGAT GATCTAAGGT 540 TCTCCAGCCA TACACATGTT TGGGTCCAGC CATTGGCACC AGGTGACTCA GCCTTTGAGC 600 CTGGCCACGC TTGGTCAGGA ACACGTGAGA TCCCCAGCAT GTGACCAAGC CTCAAGCATT 660 CATGTGGGCT GTGGACACGG AGGCTTAGAG ACAGCATAGT GGGAGCCCAG AACCACAACC 720 AGTAGCCCAA GGATTAGTGA GCCAACTGCA AGTGTGCGGA ACACAAGAGC ATCATTTTCT 780 CCTGCTCCTC CAGGGAGCTA GAAATAGAAC TCTGCCCTTT GTCCTTGAGG AGCTGAGGCA 840 ACTGCCTGGC ATGGCGTGGG TGTTGGTGAC CACAGGCCCC TTTGTTCCTC TCTCCCACTC 900 ACCCTCCCGC TCCTTCCTCG CTCCTGTGAC CCTCGGTCCC TGGCCCGTGG AGACTGTGGG 960 CAGGGCTCAG GGCCACTGGG TGGTGTCTGG GTGAAGGTGG CTGCTTAGCA CTGGCACATG 1020 TGGAGAATGT GGTGGTGAGC TCCCTCTCAG CTGCCGTTTC CTGGCCGGCA TTAGCGTTGC 1080 CACCCAAAGC CTTCCCAAGC GTGGCTGACC CTGACCTGGG GCATTCAGAA GTGTCTGGCT 1140 TCTTCCTGGC AGTAACTTCG GTGTCAGACA CGGGCCTCTA GGGTATTGTT TTTCAAATGT 1200 CATTAACTGG CCGGGCACAG TGGCTCATGT CTGTAATCCC AGCACTTTGG GAGACTGAGG 1260 CAAATGGATC AATTGAGGTC AGGAGTTCGA GACCAGCCTG ACCAACATGG TGAAACCCCA 1320 TCTCTACTAA AAATACAAAA ATTAGCCGGG GGTGGTGGCA CGTGCCTGTG ATCCCAGCTA 1380 CTTGGGAGGC 1390
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