Tag | Content |
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EnhancerAtlas ID | HS007-12996 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr5:504900-505780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYCN | MA0104.4 | chr5:505059-505071 | GGCCACGTGGGC | + | 6.27 | MYCN | MA0104.4 | chr5:505059-505071 | GGCCACGTGGGC | - | 6.27 | RREB1 | MA0073.1 | chr5:505649-505669 | ACTGGGGGGGTGGGGTGGGG | - | 7.1 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29117 | chr5:505581-507311 | Fetal_Intestine_Large |
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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 | GGCCCCTTCA TGGGGGCCGG GCCAGAGGCT CAGAAGGGGA GGGCAGGGGT GCGGCTGGTT 60 GAGTGGCATA CAGCGGGGGC TCACACCTCG GCTAGCAAAG TGGCTCCCAG ACCCGGACGC 120 CTGTGCCTGG AAGAGCAGCA GACGCCTGCA GGGCACAGTG GCCACGTGGG CGCCACACAG 180 AGCCCAGTGC TGAGAAGCAG GGGCCAGCAG CTGCCACCCC TCCCCTGCTT TCCCTGTGCA 240 AATGGGAAAA GGCCTCAGAA CAGCGTGGAC GCAGTGACCC CTTTAACAGA ATGAGGGGAT 300 GGAATCCCGG GTGGCTGGAG ACCTGGACAA ATGAGAAACA GCATCCTCCT CCATTTTTAG 360 CTTCAGAGGC TCTTAAGGGA GGGAGGCTGC TGTGGGAGGA GCATCTGGAT GTGTGCTGGG 420 GGGTGACCAT CGAGGGGGGT GGGGGAGAGT GACCATGGGG GGGGGAGAGT GACTGTGGGG 480 GGGTGGGGAG TGACCACGGG GTGAAGAGTG ACTGTAGGAG GGTGGGGAGT GACCACGGAG 540 AGGGGAGAGT GACTGTAGGG GGGTGGGGAG TGACCATGGA AGGGGGAGAG TGACTGTTGG 600 GGGGTGGGGA GTGACCGCGG GGTGAAGAGT GACTGTAGGA GGGTGGGGAG TGACCATGGA 660 AGGGGGAGAG TGACTGTTGG GGGGTGGAGA GTGACCACAG AGGGGAGAGT GACTGTGGGG 720 GGGTGGGGAG TGACCACGGG GGGAGAGTGA CTGGGGGGGT GGGGTGGGGA GTGACCACGG 780 AGGTGAGAGT GACTGTGGGG GGGTGGGGAG TGACCATGGA AGGGGGAGAG TGACTGTGGG 840 GGGTGGAGAG TGACCACAGA GGGGAGAGTG ACTGTGGGGG 880
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