| Tag | Content |
|---|
EnhancerAtlas ID | HS042-21100 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr18:33160560-33161560 | 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 | TTTTTTTTTT TTTCGGACAG CCTTTTGGTT ATGTGAGAGG TAATATAAAT TTAAAAGTGG 60
GACCACTTAA ATATTAAGTA ATCTCTTATT GCAGCTCTTG GTTGGCAAGC AATAAGACAC 120
AAACCTCTGA ATTATTTAAG TAGAAAATTA ATTTATTAAA AGAATGGTTG GTTATGCCTC 180
GCGTGAGTGA CAGAGCCAGG GTTTTGTCTT CTATCTTCAG GGCAGGGTAC AGCTGGGTAT 240
TGGAATTGTA CCAAGCAGTG TTTCCCAAGG GGGCACAGAG GGAGGGCCCC TCTCCGGGCA 300
CTGTGCGGGA GCCACTTCCC CAAACAGTCC CCGTTCTGCA AGGGCCCCGG CGTTGCTGCC 360
CCCGAGACCC GGGTGCCTGC CCCGGCGGTG CGGGTCGCGG GCCTCCGCTC TCGCCGTCCT 420
CCCTCAGTCC CGGGCCTCCT GCATCGCGGT CGCCAGGCGC AGGCTCAGCG CGGCTGACAG 480
CGCTCCAGCT CCCGCGCTCG CGGCCGCCTC AGGCAGCCGA CCGGGTTGGG GCGGCCCCGC 540
GCTCGGCCCG GGAGCCGATC CGCTGTGAGG GCTCCTCCAT CTCCTCCCAC CCCGTGACCT 600
GCTCGACGCG CAACAGCCCG AGTTGTCTTT AACTTGCTGC GGCAGCCTCT TTGTCCCGAC 660
CCAGGGTCGG GGGCACCTCT CGGCCTGGCC CGGCCCTGCC CGTAGCCGTG TGAGCGGGGG 720
CCGGGACTGG GCGGTCGGTC CGGGAGGGGC GCCGCGCCCG ACCCCGGAGT CCCGAGCCCG 780
AGGGGAGCGT CGCGGCCCCG CGGTGGGCTC GCCGCAGCGG AGGGGGCGCG CATCCGGGTG 840
AGCGCCGGCG CCCCCGCCTC CCCCGCGCAG CCGCACGGGC CGCCGCCGCC GCTGCCGCCG 900
AGCACGCAGC GCAGGGAGGA CCGCGCCCGA GCGCCTGCGG GCGCCCTGCG GCGCCCGCCG 960
CGCGACGAGC CCCAAGTGAG CGGGCAGGCG GCGCGCATGC 1000
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