| Tag | Content |
|---|
EnhancerAtlas ID | HS044-06204 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr18:33160490-33161700 | 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 | TTAGAATACT TGGAAGATGT AGACAAGCAA AAACAGGATA CTAAAATTCC AGAGATAATC 60
TTCAGGTTTT TTTTTTTTTT TTTCGGACAG CCTTTTGGTT ATGTGAGAGG TAATATAAAT 120
TTAAAAGTGG GACCACTTAA ATATTAAGTA ATCTCTTATT GCAGCTCTTG GTTGGCAAGC 180
AATAAGACAC AAACCTCTGA ATTATTTAAG TAGAAAATTA ATTTATTAAA AGAATGGTTG 240
GTTATGCCTC GCGTGAGTGA CAGAGCCAGG GTTTTGTCTT CTATCTTCAG GGCAGGGTAC 300
AGCTGGGTAT TGGAATTGTA CCAAGCAGTG TTTCCCAAGG GGGCACAGAG GGAGGGCCCC 360
TCTCCGGGCA CTGTGCGGGA GCCACTTCCC CAAACAGTCC CCGTTCTGCA AGGGCCCCGG 420
CGTTGCTGCC CCCGAGACCC GGGTGCCTGC CCCGGCGGTG CGGGTCGCGG GCCTCCGCTC 480
TCGCCGTCCT CCCTCAGTCC CGGGCCTCCT GCATCGCGGT CGCCAGGCGC AGGCTCAGCG 540
CGGCTGACAG CGCTCCAGCT CCCGCGCTCG CGGCCGCCTC AGGCAGCCGA CCGGGTTGGG 600
GCGGCCCCGC GCTCGGCCCG GGAGCCGATC CGCTGTGAGG GCTCCTCCAT CTCCTCCCAC 660
CCCGTGACCT GCTCGACGCG CAACAGCCCG AGTTGTCTTT AACTTGCTGC GGCAGCCTCT 720
TTGTCCCGAC CCAGGGTCGG GGGCACCTCT CGGCCTGGCC CGGCCCTGCC CGTAGCCGTG 780
TGAGCGGGGG CCGGGACTGG GCGGTCGGTC CGGGAGGGGC GCCGCGCCCG ACCCCGGAGT 840
CCCGAGCCCG AGGGGAGCGT CGCGGCCCCG CGGTGGGCTC GCCGCAGCGG AGGGGGCGCG 900
CATCCGGGTG AGCGCCGGCG CCCCCGCCTC CCCCGCGCAG CCGCACGGGC CGCCGCCGCC 960
GCTGCCGCCG AGCACGCAGC GCAGGGAGGA CCGCGCCCGA GCGCCTGCGG GCGCCCTGCG 1020
GCGCCCGCCG CGCGACGAGC CCCAAGTGAG CGGGCAGGCG GCGCGCATGC GGGGCGGCCC 1080
GGAGTAGCGC CGCCCGAGCC CGCGAGCGGG GCGCCCGGAG TAGCCGCCGA CCCGAGCCGG 1140
GCGCGGAGGC GGGGGCGGGC GCGGCGGAGC GGGGCCCGGC CGGACCCGCC CGCCCGCCGG 1200
GGGAGCCGCC 1210
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