Tag | Content |
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EnhancerAtlas ID | HS088-00656 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:16359020-16359660 |
Target genes | Number: 19 | 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I016032 | chr1 | 16359295 | 16359696 |
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Enhancer Sequence | GGTAACAAGT ATTGGGGAGT GTGACACACG CAGCCCCCGG GGCAGGGCAA GAGCTGATGA 60 GGAGCTCAGG CTCCAGCCTC CCGTCCCAAC CCCGCCCCGC CCATCTTATC CTGCTTCCTG 120 CTCCTCCTGG GCCTGGACAG GGCAGCTCCT GCCGTCGCCC CTCACTGCCA GGGTTGCGGG 180 GATGATGCAG AGAGATGAGG GAATTGGGGG GCTTGGCAAA TGGAAGTCTC TGGGTGGAGA 240 AAGACAGTGG AGTTGCACCA AGGCACACGT GCGTTTCAAT TTCAGGTCCA CCCCATTTTG 300 CCTGTGTGAT CTTGGACAAA TTATGTAGCC AGTTGAGACA GAGCCTGACA CAAGGATGGG 360 GCAAGGGCGG AGGCTGACAG GGGACCTGGA GATGGCCCCG CCCCCTCTGT GCTGCTGGAG 420 GGTGCTGGAT GTTGGGTCCT GTCCACTTGC AGCCCCGCCC AGACCCTTGA GTGGCCTCTG 480 GCATCCCCCA GTGGCCCACA CTGGACATTG CAGGCCTGGG TCTGTTGCCT CCCACACATA 540 TCAGGCCCCG CCCCTCTTCC TGGCTCAGAG GCGTGGCAGA GTGGGCCAGA GGGTGGGCTG 600 GGCGCCATCT ACCCTCCAGT GTTTCCTAAC AATCCCCCAT 640
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