| Tag | Content |
|---|
EnhancerAtlas ID | HS138-17854 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr18:33160500-33161410 | 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 | TGGAAGATGT AGACAAGCAA AAACAGGATA CTAAAATTCC AGAGATAATC TTCAGGTTTT 60
TTTTTTTTTT TTTCGGACAG CCTTTTGGTT ATGTGAGAGG TAATATAAAT TTAAAAGTGG 120
GACCACTTAA ATATTAAGTA ATCTCTTATT GCAGCTCTTG GTTGGCAAGC AATAAGACAC 180
AAACCTCTGA ATTATTTAAG TAGAAAATTA ATTTATTAAA AGAATGGTTG GTTATGCCTC 240
GCGTGAGTGA CAGAGCCAGG GTTTTGTCTT CTATCTTCAG GGCAGGGTAC AGCTGGGTAT 300
TGGAATTGTA CCAAGCAGTG TTTCCCAAGG GGGCACAGAG GGAGGGCCCC TCTCCGGGCA 360
CTGTGCGGGA GCCACTTCCC CAAACAGTCC CCGTTCTGCA AGGGCCCCGG CGTTGCTGCC 420
CCCGAGACCC GGGTGCCTGC CCCGGCGGTG CGGGTCGCGG GCCTCCGCTC TCGCCGTCCT 480
CCCTCAGTCC CGGGCCTCCT GCATCGCGGT CGCCAGGCGC AGGCTCAGCG CGGCTGACAG 540
CGCTCCAGCT CCCGCGCTCG CGGCCGCCTC AGGCAGCCGA CCGGGTTGGG GCGGCCCCGC 600
GCTCGGCCCG GGAGCCGATC CGCTGTGAGG GCTCCTCCAT CTCCTCCCAC CCCGTGACCT 660
GCTCGACGCG CAACAGCCCG AGTTGTCTTT AACTTGCTGC GGCAGCCTCT TTGTCCCGAC 720
CCAGGGTCGG GGGCACCTCT CGGCCTGGCC CGGCCCTGCC CGTAGCCGTG TGAGCGGGGG 780
CCGGGACTGG GCGGTCGGTC CGGGAGGGGC GCCGCGCCCG ACCCCGGAGT CCCGAGCCCG 840
AGGGGAGCGT CGCGGCCCCG CGGTGGGCTC GCCGCAGCGG AGGGGGCGCG CATCCGGGTG 900
AGCGCCGGCG 910
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