Tag | Content |
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EnhancerAtlas ID | HS082-06156 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr11:43811360-43812800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2B | MA0660.1 | chr11:43811776-43811788 | GCTAAAAATAGT | + | 6.11 | MEF2C | MA0497.1 | chr11:43811774-43811789 | AGGCTAAAAATAGTA | + | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 43811372 | 43811574 | chr11 | 43811598 | 43812265 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I043787 | chr11 | 43808809 | 43812862 |
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Enhancer Sequence | GGTCCCAGCT ACTTGGGAGG CTGAGATGGG AGGATCTCTT GAACCCAGAA GGTCCAAGCT 60 GCAATGAGCC ATGACCGCGC CACTGCACTC TAGCCTGGGT GCCAGAGTGA GACCCTGTCC 120 CACTGCCCAC TGCCTCCCCC CCGCAAAAAA GAGAGAGAAG CGTGACTGTC AGCAGGGTTC 180 CCAGGCTTCT TTCATCAAAT CTGAGATACC ATTGATCATG AAGCAACAAT GCAGCTTATA 240 ACCACTAAGA AAGAAAATTC ACCAATTAAA CTGACTTGCC ATCAATTATA AAACACCTTG 300 ATTTCAGAGA TGAAAAGTGA ACTAAAATGT ACACCTTGGA ATAGATAACA TACAATAATT 360 TAAAGGTTAA TTACAAGCAA ATTGAGTCAA GGAAATACTT GGACGCTAAA AGCAAGGCTA 420 AAAATAGTAC ATCATGACCA TTGATTCCAT GGATGATATG GTAATGAATC ACTTTTTGAA 480 GCAGAGTCAG ATGTTCATGC CAGCTTGAAA AAATATGCAG CTGATGCAAG GAGGTAAGAG 540 TTAAGAATAC AGATTATACC TACAGCAGCC TATGCTATTA AGGAAAAAAC AACTATTTGC 600 CAAGCAGCCA TCTTTGTAGA TATTGGCAGA TAGAGGAGTC CCCCCCGTGT CTGCAGGGGA 660 TATGCCACAA GATCCCCAGT GAATACTTGA AACTGTGGAT AGTGCTGAAC CCTATATACC 720 TATATGTGCT CTTTTTCTGA TCTGATAACC AAGAGAGATA CTAAGTGACT AAAGAGTGGG 780 TGGTGTGTAC AGCATGGATA TGCTGGACAA AGGTATGATT CACACTGAGA GCAGGACAGT 840 GCAAGATTTC ATCATGCTAA TTAGAATGGC GTGCAATTTA AAACTTATGA ATTATTATGG 900 GCCAGGCACA GTGGCTTACG CCTGTAATCC CAGCACTTTG GGAGGCTGAG GCAGGCGGAT 960 CACCTGAGGT CAGGAGTTTG AGACCAGCCT GGCCAACATG GTGAAACCCC ATCTCTAATA 1020 AAAAAATACA AAAATTAACA GGGCATGGTA GTGGGTGCCT GTAATCCCAG CTACTCGGAA 1080 GGCTGAGGCA GGAGAATCGC TTGAACCCAG GAGGTGGAGG TTGCAGTGAG CCAAGATTGC 1140 ACCATTGCAT TCCAGCCTGG GCAACAAAAG CGGAACTCCA TCTCAAAAAA ACAAAAAACA 1200 AAATAAAAAA AAACTGTGTA GGGTGGGTAT TATTTTTTGT GGTTTTCTAG GCTAAGAAAT 1260 GGTATTCTTG AAAGTTCAAA GGCTTGAGTG AAGGGCCTTA GGCCAGCAAC CAGTTGAGTT 1320 GGCACTCAAG TGCAGGTCTT CTAACTGCAT CCCAGGCTCT TCCAGTGAAC CCTGCTTTCA 1380 TACTGCTAGC AGTAGCATCT TGGAATCTTA AGTGTAGTAA TCTTAAGAAT GATGTTTTGG 1440
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