| Tag | Content |
|---|
EnhancerAtlas ID | HS062-16875 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr9:138859000-138859980 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr9:138859557-138859576 | CAGCCACTAGAGGGTGCAG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH09I135967 | chr9 | 138858910 | 138860046 |
| Enhancer Sequence | AGGAGCAGGC TCCGCGGCGG TGGCGTCAGC CCTCGGAACT CCCTGCAGCT CTCAGGAAGG 60
GGCAGGCCAG GTGCGTTGTC CTGGAGCTGC CTGCCAGTTC CCCCTGCCTC GTTTGGTCTG 120
GGCGTAGCTG CCCAAGGCCC TGCAGGGAAT CAGCGAAGGC CCAGGTGACA GATTCCCTGC 180
ATCTGCAGGG GCAGAGCCAG TCCTGGCCCG AGGCCTGGAG TGAGGCCACC CCAGCCTGCC 240
CTGGCTCTTG CCATGGCCCT GAGAGTTCCC TGGAGGAGCC CCAGCTGCCC TGGGTGGTGG 300
CAGCTAAGGA CAAGGCCATC CTGCCCACGG TCTCCCCGAC CCCTGCCTCG ACTTAGCTCC 360
CTGGGCAGAT GTGGCCAGAG CCCCCAGCCC CCGTATGGTG TCAGCGCCTG GCTGGGCAGG 420
CCAAGCAGGG TCTCCTGGCA AAGGGGGCTC CAAGTGTGAC TGAGGTGGGG TGTGCCGCTC 480
TCATCCACTG CACCCCCAGG TGGCCTGGAC CCAACCCGAA ACTCAACAAG CAGCAGCCTG 540
GCCGTGGTGC CTCAAGCCAG CCACTAGAGG GTGCAGTTGA GCTGTCAGCC TGCCTGGAGG 600
GGCGAGGTGG TGGGGGTGAG TGTGCAGGCG TGTGTGTGTG TGTGTGTGTG TGTGCGCGCG 660
CGCGCGCGCC TGTGTGTGGG CGTGTTGTGT GCATGTGTGC ATATGTGTGC ACTGTGTATA 720
TGTGCCATGT GTATGCGTGC ATGTGTCCGT GTGTGTATAT GTGTGCGTGT GCATGTGTGC 780
CATGTATGCA TATGTGTGCA TGTTCATGTG TGCGGGGGGG TGTGCACCTG TGTGTGGGCG 840
TGTTGTGTGC ATGTGTGCAC TGTGCATATG TGCTGTGTGT GTGCATGCAT ATGTCTGCAT 900
GCATGTGTGT GTGCCATGTA TGCATATGTG TGCATGTTTA TGTGGGGGGG TGTGCATGTT 960
GCTGTGCATG TATATATGGG 980
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