| Tag | Content |
|---|
EnhancerAtlas ID | HS095-13733 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr18:33160590-33161700 | 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 | ATGTGAGAGG TAATATAAAT TTAAAAGTGG GACCACTTAA ATATTAAGTA ATCTCTTATT 60
GCAGCTCTTG GTTGGCAAGC AATAAGACAC AAACCTCTGA ATTATTTAAG TAGAAAATTA 120
ATTTATTAAA AGAATGGTTG GTTATGCCTC GCGTGAGTGA CAGAGCCAGG GTTTTGTCTT 180
CTATCTTCAG GGCAGGGTAC AGCTGGGTAT TGGAATTGTA CCAAGCAGTG TTTCCCAAGG 240
GGGCACAGAG GGAGGGCCCC TCTCCGGGCA CTGTGCGGGA GCCACTTCCC CAAACAGTCC 300
CCGTTCTGCA AGGGCCCCGG CGTTGCTGCC CCCGAGACCC GGGTGCCTGC CCCGGCGGTG 360
CGGGTCGCGG GCCTCCGCTC TCGCCGTCCT CCCTCAGTCC CGGGCCTCCT GCATCGCGGT 420
CGCCAGGCGC AGGCTCAGCG CGGCTGACAG CGCTCCAGCT CCCGCGCTCG CGGCCGCCTC 480
AGGCAGCCGA CCGGGTTGGG GCGGCCCCGC GCTCGGCCCG GGAGCCGATC CGCTGTGAGG 540
GCTCCTCCAT CTCCTCCCAC CCCGTGACCT GCTCGACGCG CAACAGCCCG AGTTGTCTTT 600
AACTTGCTGC GGCAGCCTCT TTGTCCCGAC CCAGGGTCGG GGGCACCTCT CGGCCTGGCC 660
CGGCCCTGCC CGTAGCCGTG TGAGCGGGGG CCGGGACTGG GCGGTCGGTC CGGGAGGGGC 720
GCCGCGCCCG ACCCCGGAGT CCCGAGCCCG AGGGGAGCGT CGCGGCCCCG CGGTGGGCTC 780
GCCGCAGCGG AGGGGGCGCG CATCCGGGTG AGCGCCGGCG CCCCCGCCTC CCCCGCGCAG 840
CCGCACGGGC CGCCGCCGCC GCTGCCGCCG AGCACGCAGC GCAGGGAGGA CCGCGCCCGA 900
GCGCCTGCGG GCGCCCTGCG GCGCCCGCCG CGCGACGAGC CCCAAGTGAG CGGGCAGGCG 960
GCGCGCATGC GGGGCGGCCC GGAGTAGCGC CGCCCGAGCC CGCGAGCGGG GCGCCCGGAG 1020
TAGCCGCCGA CCCGAGCCGG GCGCGGAGGC GGGGGCGGGC GCGGCGGAGC GGGGCCCGGC 1080
CGGACCCGCC CGCCCGCCGG GGGAGCCGCC 1110
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