| Tag | Content |
|---|
EnhancerAtlas ID | HS193-15388 | Organism | Homo sapiens | Tissue/cell | U87 | Coordinate | chr18:33160610-33161700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr18:33160704-33160717 | AAATTAATTTATT | + | 6 | | TFAP2A | MA0003.3 | chr18:33161064-33161075 | CGCCTCAGGCA | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTAAAAGTGG GACCACTTAA ATATTAAGTA ATCTCTTATT GCAGCTCTTG GTTGGCAAGC 60
AATAAGACAC AAACCTCTGA ATTATTTAAG TAGAAAATTA ATTTATTAAA AGAATGGTTG 120
GTTATGCCTC GCGTGAGTGA CAGAGCCAGG GTTTTGTCTT CTATCTTCAG GGCAGGGTAC 180
AGCTGGGTAT TGGAATTGTA CCAAGCAGTG TTTCCCAAGG GGGCACAGAG GGAGGGCCCC 240
TCTCCGGGCA CTGTGCGGGA GCCACTTCCC CAAACAGTCC CCGTTCTGCA AGGGCCCCGG 300
CGTTGCTGCC CCCGAGACCC GGGTGCCTGC CCCGGCGGTG CGGGTCGCGG GCCTCCGCTC 360
TCGCCGTCCT CCCTCAGTCC CGGGCCTCCT GCATCGCGGT CGCCAGGCGC AGGCTCAGCG 420
CGGCTGACAG CGCTCCAGCT CCCGCGCTCG CGGCCGCCTC AGGCAGCCGA CCGGGTTGGG 480
GCGGCCCCGC GCTCGGCCCG GGAGCCGATC CGCTGTGAGG GCTCCTCCAT CTCCTCCCAC 540
CCCGTGACCT GCTCGACGCG CAACAGCCCG AGTTGTCTTT AACTTGCTGC GGCAGCCTCT 600
TTGTCCCGAC CCAGGGTCGG GGGCACCTCT CGGCCTGGCC CGGCCCTGCC CGTAGCCGTG 660
TGAGCGGGGG CCGGGACTGG GCGGTCGGTC CGGGAGGGGC GCCGCGCCCG ACCCCGGAGT 720
CCCGAGCCCG AGGGGAGCGT CGCGGCCCCG CGGTGGGCTC GCCGCAGCGG AGGGGGCGCG 780
CATCCGGGTG AGCGCCGGCG CCCCCGCCTC CCCCGCGCAG CCGCACGGGC CGCCGCCGCC 840
GCTGCCGCCG AGCACGCAGC GCAGGGAGGA CCGCGCCCGA GCGCCTGCGG GCGCCCTGCG 900
GCGCCCGCCG CGCGACGAGC CCCAAGTGAG CGGGCAGGCG GCGCGCATGC GGGGCGGCCC 960
GGAGTAGCGC CGCCCGAGCC CGCGAGCGGG GCGCCCGGAG TAGCCGCCGA CCCGAGCCGG 1020
GCGCGGAGGC GGGGGCGGGC GCGGCGGAGC GGGGCCCGGC CGGACCCGCC CGCCCGCCGG 1080
GGGAGCCGCC 1090
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