| Tag | Content |
|---|
EnhancerAtlas ID | HS082-15895 | Organism | Homo sapiens | Tissue/cell | HCASMC | Coordinate | chr18:33160540-33161700 | 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 | AGAGATAATC TTCAGGTTTT TTTTTTTTTT TTTCGGACAG CCTTTTGGTT ATGTGAGAGG 60
TAATATAAAT TTAAAAGTGG GACCACTTAA ATATTAAGTA ATCTCTTATT GCAGCTCTTG 120
GTTGGCAAGC AATAAGACAC AAACCTCTGA ATTATTTAAG TAGAAAATTA ATTTATTAAA 180
AGAATGGTTG GTTATGCCTC GCGTGAGTGA CAGAGCCAGG GTTTTGTCTT CTATCTTCAG 240
GGCAGGGTAC AGCTGGGTAT TGGAATTGTA CCAAGCAGTG TTTCCCAAGG GGGCACAGAG 300
GGAGGGCCCC TCTCCGGGCA CTGTGCGGGA GCCACTTCCC CAAACAGTCC CCGTTCTGCA 360
AGGGCCCCGG CGTTGCTGCC CCCGAGACCC GGGTGCCTGC CCCGGCGGTG CGGGTCGCGG 420
GCCTCCGCTC TCGCCGTCCT CCCTCAGTCC CGGGCCTCCT GCATCGCGGT CGCCAGGCGC 480
AGGCTCAGCG CGGCTGACAG CGCTCCAGCT CCCGCGCTCG CGGCCGCCTC AGGCAGCCGA 540
CCGGGTTGGG GCGGCCCCGC GCTCGGCCCG GGAGCCGATC CGCTGTGAGG GCTCCTCCAT 600
CTCCTCCCAC CCCGTGACCT GCTCGACGCG CAACAGCCCG AGTTGTCTTT AACTTGCTGC 660
GGCAGCCTCT TTGTCCCGAC CCAGGGTCGG GGGCACCTCT CGGCCTGGCC CGGCCCTGCC 720
CGTAGCCGTG TGAGCGGGGG CCGGGACTGG GCGGTCGGTC CGGGAGGGGC GCCGCGCCCG 780
ACCCCGGAGT CCCGAGCCCG AGGGGAGCGT CGCGGCCCCG CGGTGGGCTC GCCGCAGCGG 840
AGGGGGCGCG CATCCGGGTG AGCGCCGGCG CCCCCGCCTC CCCCGCGCAG CCGCACGGGC 900
CGCCGCCGCC GCTGCCGCCG AGCACGCAGC GCAGGGAGGA CCGCGCCCGA GCGCCTGCGG 960
GCGCCCTGCG GCGCCCGCCG CGCGACGAGC CCCAAGTGAG CGGGCAGGCG GCGCGCATGC 1020
GGGGCGGCCC GGAGTAGCGC CGCCCGAGCC CGCGAGCGGG GCGCCCGGAG TAGCCGCCGA 1080
CCCGAGCCGG GCGCGGAGGC GGGGGCGGGC GCGGCGGAGC GGGGCCCGGC CGGACCCGCC 1140
CGCCCGCCGG GGGAGCCGCC 1160
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