Tag | Content |
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EnhancerAtlas ID | HS105-00873 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:16359030-16359660 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr1:16359414-16359425 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:16359414-16359424 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:16359564-16359574 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr1:16359561-16359576 | CAGGCCCCGCCCCTC | + | 6.22 | SP1 | MA0079.4 | chr1:16359411-16359426 | ATGGCCCCGCCCCCT | + | 6.39 | SP4 | MA0685.1 | chr1:16359561-16359578 | CAGGCCCCGCCCCTCTT | + | 6.52 | SP4 | MA0685.1 | chr1:16359411-16359428 | ATGGCCCCGCCCCCTCT | + | 6.97 |
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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 |
GH01I016032 | chr1 | 16359295 | 16359696 |
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Enhancer Sequence | ATTGGGGAGT GTGACACACG CAGCCCCCGG GGCAGGGCAA GAGCTGATGA GGAGCTCAGG 60 CTCCAGCCTC CCGTCCCAAC CCCGCCCCGC CCATCTTATC CTGCTTCCTG CTCCTCCTGG 120 GCCTGGACAG GGCAGCTCCT GCCGTCGCCC CTCACTGCCA GGGTTGCGGG GATGATGCAG 180 AGAGATGAGG GAATTGGGGG GCTTGGCAAA TGGAAGTCTC TGGGTGGAGA AAGACAGTGG 240 AGTTGCACCA AGGCACACGT GCGTTTCAAT TTCAGGTCCA CCCCATTTTG CCTGTGTGAT 300 CTTGGACAAA TTATGTAGCC AGTTGAGACA GAGCCTGACA CAAGGATGGG GCAAGGGCGG 360 AGGCTGACAG GGGACCTGGA GATGGCCCCG CCCCCTCTGT GCTGCTGGAG GGTGCTGGAT 420 GTTGGGTCCT GTCCACTTGC AGCCCCGCCC AGACCCTTGA GTGGCCTCTG GCATCCCCCA 480 GTGGCCCACA CTGGACATTG CAGGCCTGGG TCTGTTGCCT CCCACACATA TCAGGCCCCG 540 CCCCTCTTCC TGGCTCAGAG GCGTGGCAGA GTGGGCCAGA GGGTGGGCTG GGCGCCATCT 600 ACCCTCCAGT GTTTCCTAAC AATCCCCCAT 630
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