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EnhancerAtlas ID | HS034-10769 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr16:1842520-1843080 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr16:1842606-1842616 | GCCCCGCCCC | + | 6.02 | MYCN | MA0104.4 | chr16:1842657-1842669 | GGCCACGTGGGC | + | 6.27 | MYCN | MA0104.4 | chr16:1842657-1842669 | GGCCACGTGGGC | - | 6.27 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GATGCGAAGA AGCCGGTGAG CCCCACAGGT CCTCCGGCTC AAAAGCTGAC ACTGCGCTTC 60 CCACCCCATG GGACAGAGGA GTGGCCGCCC CGCCCCGCTG CACAGACGCT CAGGGCTTGG 120 CTCTCCAGCT GTGCGCAGGC CACGTGGGCT CGGCCAGGCT GGGTCTCGGG CTGTCTGGCC 180 ATGTGGCAGC CGCACCCCCA AGGCAGGCGC TTGAGCCAGG CCAGTCTGCC ACGTTGGCCT 240 AGAGGAAGGG GAGGGAACTG AGCCATTGGC CAAGGTCCGG CCATTTTCAG AATATTCTGC 300 AGCAGGTCTT GGTGGGCACT CGCTCACTGC CCTCAGAGGC TGGACAGGGA GCTGGGCACC 360 TCCTGCCCCA GTTAGGCCCC CCAGCGGGGT CTCACCTGCC TGCATCCAGG CCTTGGTCGG 420 GTGCTGCGGG AGGGGACCGG GGCACCGCCG TCGGGGGACA GGTAGGAACC CTGGACCGTC 480 GGCCACCAAA GCTCACATTG CCTTTCAGGA CAAGGGGCCA CAGGCCCCAC AGACCCAGCC 540 AGCAGGCTCC CAAGCAGCGA 560
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