Tag | Content |
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EnhancerAtlas ID | HS111-01052 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr11:117015140-117016120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr11:117015973-117015984 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr11:117015973-117015984 | GGTGACTCATG | + | 6.02 | KLF5 | MA0599.1 | chr11:117015453-117015463 | GCCCCGCCCC | + | 6.02 |
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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 | GCATCCAGGG TCGCAGGGAA CCGGTGGCTT AGAGGCGGGG GTCGGAAGGG GCTGCGAGGT 60 GTTATTGTGA GAGGCCCGCG ACCTCCCCTC CCCCACCCTT GCGGCCCCTC CCCCCACGCC 120 GCCCCATCCA CTTGGGGGGG GCCTCGCGAG CGCGCGCCTT CTCTGCGGGC CCAGCGTCGG 180 CTTCCCAGCA GCCGGCGCAG CTAGTTTTCG CTCTGAGAGC CCTTTCCCGA TATTCCATAC 240 CGAAAGCTGG CGTTTCTCCT CAGCCGCCGG CCGGCGCCTC CACGGCCTTT CCCAGGAGGG 300 TAGCGCGGCG GGCGCCCCGC CCCGCCCTGC CCTGCCCTGC CCTGCCGGGC CCACCCGCGG 360 TAGGCCTTGC GCACCCCAGC TCGCCCCGGC TGGGCGCTGC AGCTCCTGCC CGGGTCTCCG 420 CTGCTGCCTT TTCCCTTTAT CACAGGGGTC TAACTTCTCA CTCTTCTCTC CCCTCGCGTC 480 TGGTCGGAGG CCAAAACCAG TTACTCCGTT GTGTTTTTAC CGAGCACTTT TCCCTCCTCC 540 TTTTGTTGAA AAATTTCAAC TCTTTAGAAA CTTCTCCGTT GCCTCTTAGG ATGTGTTTAT 600 TCAAAAGTTG CATAGACCGT CACCACTCGG AAGGGATTAT TTCTTGGAAG GCTTTCCAGC 660 CCCCATCTCA TCTTAGACAT GAATGTGCTC GGAGCGGCTG GTGACCTGCC CAAGGTCAGC 720 CAGCTAGATA AACCTGTCAG CGGAGAGGTT TGGGGGGATG TTTTTTTCCT GGCTCACCGT 780 CCGTTTGCCA GATCCGTGCC TTCTGGTCTA CAGGTTTGAT TGACCCGTTG CGTGGTGACT 840 CATGCTTCTG CTTTTCATAG CTCGCAGGCC AGCGTTGCTT TTCAGAATTT ATACACAAAC 900 AAGAACTAAC ACTCGGAGCT TTCGCCTCTT TGTAGAGCTT ACCCGTAGAG AAAGGAAAGA 960 CCACCCGGAT CCACCCTAGG 980
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