Tag | Content |
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EnhancerAtlas ID | HS044-02281 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr11:18033590-18034490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr11:18034225-18034237 | TGCCCCGAGGCA | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35602 | chr11:18032257-18034670 | HepG2 |
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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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Enhancer Sequence | ATTTCCCCAA CACCAGCACA TGGGTAGGCA CACAGATGCT CGTTCATTCA TTCGTCAACG 60 AGTATTTACT GGGGACCTAC AATGTGCCAG ACACCAAGAG AGGCACCGTG AACAAGACAG 120 GCACAGCACC CACTCTTACC ACACTTACTT TCCAGCCAGA GAGACTGACG TTAATAATAA 180 ATTATACACA TCATTACAAT TGTGATACGT GCTATGAAGA AGCACAAGAC GCAGCGACTG 240 CTTGTTCCCG TGCATGCTGG TCGGCCACCT GCCACGCTCC TGTGCATGAA CCCTCCTCTC 300 TCCCAGACAC ACATCAAGAT GACCCTGTCT CTCCCAATGC TCCCGTCAAA CCAACAGCAG 360 CCCAACTCCC CCAACACATG CAAGAACCGG TCACAGCAGA GTGTCAGCAA ATAGGCAGGG 420 TCTGTGCCTT GTGCGCGGCC AAACACCGCA GGCCTCACAT CTAAAGGATG CTTTCGCCAG 480 GCTGGGACAG GGTCTCCCTC CTCCAGGCAT CAGGAGTGTG GGGGGCACAG GTGGCCCCAC 540 GGAGCTCTGG GACCGGGCGA TCCTCTCCAC CGAGCCCTCC GCGCTGTCTT CCAGGCGCTA 600 TTCGGGCTGG AGGGCTCTCG CGGAACCAGA CGCTCTGCCC CGAGGCAGGT TCTTCCCGCG 660 GCGCCACAGC CCCTCCGGCC CTGACCCCGC CAGCCGGCAG GCCCCTAAGT CGACCGCGAA 720 GACCCTTCCT TCCCCGCCCG CCCGCTCCTC CTCCGCTCCC CCTCCGCTCC CAGCCCAGGA 780 TCCTTCAACC CAGAGCCCGG CTCGGACCTC AGCCGCCCAG CCCCTGAACT GCCCACGCCG 840 CGGCCAGCAG CTCCCACATC TCGGCGCCCC TCAGGGCCTG CACCGGCCCG GGGGCGGAGT 900
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